Protein ID | Hirsu2|5820 |
Gene name | |
Location | Contig_294:11074..12082 |
Strand | - |
Gene length (bp) | 1008 |
Transcript length (bp) | 939 |
Coding sequence length (bp) | 939 |
Protein length (aa) | 313 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00753 | Lactamase_B | Metallo-beta-lactamase superfamily | 5.8E-14 | 58 | 184 |
PF12706 | Lactamase_B_2 | Beta-lactamase superfamily domain | 2.2E-06 | 71 | 180 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q99KR3|LACB2_MOUSE | Beta-lactamase-like protein 2 OS=Mus musculus GN=Lactb2 PE=1 SV=1 | 34 | 309 | 5.0E-51 |
sp|Q1LZ83|LACB2_BOVIN | Beta-lactamase-like protein 2 OS=Bos taurus GN=LACTB2 PE=2 SV=1 | 34 | 306 | 1.0E-50 |
sp|Q561R9|LACB2_RAT | Beta-lactamase-like protein 2 OS=Rattus norvegicus GN=Lactb2 PE=2 SV=1 | 34 | 306 | 3.0E-50 |
sp|Q53H82|LACB2_HUMAN | Beta-lactamase-like protein 2 OS=Homo sapiens GN=LACTB2 PE=1 SV=2 | 34 | 265 | 3.0E-50 |
sp|Q5XGR8|LACB2_XENLA | Beta-lactamase-like protein 2 OS=Xenopus laevis GN=lactb2 PE=2 SV=1 | 31 | 308 | 7.0E-50 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q99KR3|LACB2_MOUSE | Beta-lactamase-like protein 2 OS=Mus musculus GN=Lactb2 PE=1 SV=1 | 34 | 309 | 5.0E-51 |
sp|Q1LZ83|LACB2_BOVIN | Beta-lactamase-like protein 2 OS=Bos taurus GN=LACTB2 PE=2 SV=1 | 34 | 306 | 1.0E-50 |
sp|Q561R9|LACB2_RAT | Beta-lactamase-like protein 2 OS=Rattus norvegicus GN=Lactb2 PE=2 SV=1 | 34 | 306 | 3.0E-50 |
sp|Q53H82|LACB2_HUMAN | Beta-lactamase-like protein 2 OS=Homo sapiens GN=LACTB2 PE=1 SV=2 | 34 | 265 | 3.0E-50 |
sp|Q5XGR8|LACB2_XENLA | Beta-lactamase-like protein 2 OS=Xenopus laevis GN=lactb2 PE=2 SV=1 | 31 | 308 | 7.0E-50 |
sp|Q0V9A9|LACB2_XENTR | Beta-lactamase-like protein 2 OS=Xenopus tropicalis GN=lactb2 PE=2 SV=1 | 31 | 308 | 2.0E-49 |
sp|Q6NYF0|LACB2_DANRE | Beta-lactamase-like protein 2 OS=Danio rerio GN=lactb2 PE=2 SV=1 | 34 | 244 | 2.0E-48 |
sp|Q95Q18|LACB2_CAEEL | Beta-lactamase-like protein 2 homolog OS=Caenorhabditis elegans GN=Y53F4B.39 PE=3 SV=1 | 31 | 295 | 1.0E-46 |
sp|Q9VLS9|LACB2_DROME | Beta-lactamase-like protein 2 homolog OS=Drosophila melanogaster GN=CG12375 PE=2 SV=1 | 37 | 265 | 2.0E-35 |
sp|A0Q7M7|GLO2_FRATN | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. novicida (strain U112) GN=gloB PE=3 SV=1 | 70 | 222 | 2.0E-19 |
sp|Q0BMS2|GLO2_FRATO | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. holarctica (strain OSU18) GN=gloB PE=3 SV=1 | 70 | 222 | 3.0E-19 |
sp|Q2A4E2|GLO2_FRATH | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. holarctica (strain LVS) GN=gloB PE=3 SV=1 | 70 | 222 | 3.0E-19 |
sp|A7NB16|GLO2_FRATF | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. holarctica (strain FTNF002-00 / FTA) GN=gloB PE=3 SV=1 | 70 | 222 | 3.0E-19 |
sp|B0TXY0|GLO2_FRAP2 | Hydroxyacylglutathione hydrolase OS=Francisella philomiragia subsp. philomiragia (strain ATCC 25017) GN=gloB PE=3 SV=1 | 84 | 215 | 7.0E-18 |
sp|A4IWV0|GLO2_FRATW | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. tularensis (strain WY96-3418) GN=gloB PE=3 SV=1 | 70 | 222 | 8.0E-18 |
sp|Q5NF43|GLO2_FRATT | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. tularensis (strain SCHU S4 / Schu 4) GN=gloB PE=3 SV=1 | 70 | 222 | 8.0E-18 |
sp|B2SFR3|GLO2_FRATM | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. mediasiatica (strain FSC147) GN=gloB PE=3 SV=1 | 70 | 222 | 8.0E-18 |
sp|Q14GJ6|GLO2_FRAT1 | Hydroxyacylglutathione hydrolase OS=Francisella tularensis subsp. tularensis (strain FSC 198) GN=gloB PE=3 SV=1 | 70 | 222 | 8.0E-18 |
sp|Q13F06|GLO2_RHOPS | Hydroxyacylglutathione hydrolase OS=Rhodopseudomonas palustris (strain BisB5) GN=gloB PE=3 SV=1 | 72 | 190 | 2.0E-13 |
sp|Q2J429|GLO2_RHOP2 | Hydroxyacylglutathione hydrolase OS=Rhodopseudomonas palustris (strain HaA2) GN=gloB PE=3 SV=1 | 72 | 190 | 1.0E-12 |
sp|Q07VA9|GLO2_RHOP5 | Hydroxyacylglutathione hydrolase OS=Rhodopseudomonas palustris (strain BisA53) GN=gloB PE=3 SV=1 | 91 | 190 | 4.0E-12 |
sp|Q6NC62|GLO2_RHOPA | Hydroxyacylglutathione hydrolase OS=Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) GN=gloB PE=3 SV=1 | 76 | 190 | 4.0E-12 |
sp|Q6P963|GLO2_DANRE | Hydroxyacylglutathione hydrolase, mitochondrial OS=Danio rerio GN=hagh PE=2 SV=2 | 72 | 238 | 7.0E-12 |
sp|Q99KB8|GLO2_MOUSE | Hydroxyacylglutathione hydrolase, mitochondrial OS=Mus musculus GN=Hagh PE=1 SV=2 | 72 | 241 | 3.0E-11 |
sp|B4F6K2|GLO2_XENTR | Hydroxyacylglutathione hydrolase, mitochondrial OS=Xenopus tropicalis GN=hagh PE=2 SV=1 | 72 | 237 | 3.0E-11 |
sp|Q3SVQ1|GLO2_NITWN | Hydroxyacylglutathione hydrolase OS=Nitrobacter winogradskyi (strain Nb-255 / ATCC 25391) GN=gloB PE=3 SV=1 | 76 | 190 | 7.0E-11 |
sp|Q89XT5|GLO2_BRADU | Hydroxyacylglutathione hydrolase OS=Bradyrhizobium diazoefficiens (strain JCM 10833 / IAM 13628 / NBRC 14792 / USDA 110) GN=gloB PE=3 SV=1 | 76 | 190 | 8.0E-11 |
sp|O94250|GLO22_SCHPO | Probable hydroxyacylglutathione hydrolase C13B11.03c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPCC13B11.03c PE=3 SV=1 | 86 | 215 | 1.0E-10 |
sp|Q87MG0|GLO2_VIBPA | Hydroxyacylglutathione hydrolase OS=Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) GN=gloB PE=3 SV=1 | 84 | 190 | 1.0E-10 |
sp|O35952|GLO2_RAT | Hydroxyacylglutathione hydrolase, mitochondrial OS=Rattus norvegicus GN=Hagh PE=1 SV=2 | 72 | 241 | 2.0E-10 |
sp|Q3B7M2|GLO2_BOVIN | Hydroxyacylglutathione hydrolase, mitochondrial OS=Bos taurus GN=HAGH PE=2 SV=3 | 72 | 238 | 3.0E-10 |
sp|Q31H51|GLO2_THICR | Hydroxyacylglutathione hydrolase OS=Thiomicrospira crunogena (strain XCL-2) GN=gloB PE=3 SV=1 | 84 | 255 | 3.0E-10 |
sp|A4YKS8|GLO2_BRASO | Hydroxyacylglutathione hydrolase OS=Bradyrhizobium sp. (strain ORS278) GN=gloB PE=3 SV=1 | 76 | 190 | 9.0E-10 |
sp|Q4R6C1|GLO2_MACFA | Hydroxyacylglutathione hydrolase, mitochondrial OS=Macaca fascicularis GN=HAGH PE=2 SV=2 | 72 | 238 | 9.0E-10 |
sp|B6EJV4|GLO2_ALISL | Hydroxyacylglutathione hydrolase OS=Aliivibrio salmonicida (strain LFI1238) GN=gloB PE=3 SV=1 | 79 | 187 | 1.0E-09 |
sp|B2FR57|GLO2_STRMK | Hydroxyacylglutathione hydrolase OS=Stenotrophomonas maltophilia (strain K279a) GN=gloB PE=3 SV=1 | 90 | 255 | 1.0E-09 |
sp|Q16775|GLO2_HUMAN | Hydroxyacylglutathione hydrolase, mitochondrial OS=Homo sapiens GN=HAGH PE=1 SV=2 | 72 | 238 | 1.0E-09 |
sp|B4SLN7|GLO2_STRM5 | Hydroxyacylglutathione hydrolase OS=Stenotrophomonas maltophilia (strain R551-3) GN=gloB PE=3 SV=1 | 90 | 255 | 2.0E-09 |
sp|Q9UT36|GLO21_SCHPO | Probable hydroxyacylglutathione hydrolase C824.07 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC824.07 PE=3 SV=1 | 94 | 186 | 2.0E-09 |
sp|A5GJK5|GLO2_SYNPW | Hydroxyacylglutathione hydrolase OS=Synechococcus sp. (strain WH7803) GN=gloB PE=3 SV=1 | 57 | 187 | 2.0E-09 |
sp|Q5ZLY2|HAGHL_CHICK | Hydroxyacylglutathione hydrolase-like protein OS=Gallus gallus GN=HAGHL PE=2 SV=1 | 56 | 255 | 2.0E-09 |
sp|Q60BX0|GLO2_METCA | Hydroxyacylglutathione hydrolase OS=Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) GN=gloB PE=3 SV=1 | 76 | 285 | 2.0E-09 |
sp|A4W6V2|GLO2_ENT38 | Hydroxyacylglutathione hydrolase OS=Enterobacter sp. (strain 638) GN=gloB PE=3 SV=1 | 57 | 187 | 3.0E-09 |
sp|Q3IIR9|GLO2_PSEHT | Hydroxyacylglutathione hydrolase OS=Pseudoalteromonas haloplanktis (strain TAC 125) GN=gloB PE=3 SV=1 | 74 | 187 | 3.0E-09 |
sp|Q5E3G3|GLO2_VIBF1 | Hydroxyacylglutathione hydrolase OS=Vibrio fischeri (strain ATCC 700601 / ES114) GN=gloB PE=3 SV=2 | 90 | 247 | 4.0E-09 |
sp|A7MY07|GLO2_VIBCB | Hydroxyacylglutathione hydrolase OS=Vibrio campbellii (strain ATCC BAA-1116 / BB120) GN=gloB PE=3 SV=1 | 84 | 190 | 4.0E-09 |
sp|Q21C03|GLO2_RHOPB | Hydroxyacylglutathione hydrolase OS=Rhodopseudomonas palustris (strain BisB18) GN=gloB PE=3 SV=1 | 76 | 190 | 4.0E-09 |
sp|Q65U07|GLO2_MANSM | Hydroxyacylglutathione hydrolase OS=Mannheimia succiniciproducens (strain MBEL55E) GN=gloB PE=3 SV=1 | 80 | 222 | 4.0E-09 |
sp|B5F9V3|GLO2_VIBFM | Hydroxyacylglutathione hydrolase OS=Vibrio fischeri (strain MJ11) GN=gloB PE=3 SV=1 | 90 | 247 | 5.0E-09 |
sp|Q1QQZ1|GLO2_NITHX | Hydroxyacylglutathione hydrolase OS=Nitrobacter hamburgensis (strain X14 / DSM 10229) GN=gloB PE=3 SV=1 | 87 | 190 | 6.0E-09 |
sp|A7YY46|PNKD_BOVIN | Probable hydrolase PNKD OS=Bos taurus GN=PNKD PE=2 SV=1 | 72 | 254 | 6.0E-09 |
sp|Q7VD23|GLO2_PROMA | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain SARG / CCMP1375 / SS120) GN=gloB PE=3 SV=1 | 70 | 186 | 7.0E-09 |
sp|Q5ZI23|GLO2_CHICK | Hydroxyacylglutathione hydrolase, mitochondrial OS=Gallus gallus GN=HAGH PE=2 SV=1 | 72 | 187 | 9.0E-09 |
sp|Q5N5S6|GLO2_SYNP6 | Hydroxyacylglutathione hydrolase OS=Synechococcus sp. (strain ATCC 27144 / PCC 6301 / SAUG 1402/1) GN=gloB PE=3 SV=2 | 72 | 187 | 1.0E-08 |
sp|Q31ND6|GLO2_SYNE7 | Hydroxyacylglutathione hydrolase OS=Synechococcus elongatus (strain PCC 7942) GN=gloB PE=3 SV=1 | 72 | 187 | 1.0E-08 |
sp|Q6PII5|HAGHL_HUMAN | Hydroxyacylglutathione hydrolase-like protein OS=Homo sapiens GN=HAGHL PE=2 SV=1 | 95 | 203 | 2.0E-08 |
sp|Q9PBI4|GLO2_XYLFA | Hydroxyacylglutathione hydrolase OS=Xylella fastidiosa (strain 9a5c) GN=gloB PE=3 SV=1 | 92 | 203 | 2.0E-08 |
sp|Q87C74|GLO2_XYLFT | Hydroxyacylglutathione hydrolase OS=Xylella fastidiosa (strain Temecula1 / ATCC 700964) GN=gloB PE=3 SV=1 | 92 | 203 | 2.0E-08 |
sp|B2I5S5|GLO2_XYLF2 | Hydroxyacylglutathione hydrolase OS=Xylella fastidiosa (strain M23) GN=gloB PE=3 SV=1 | 92 | 203 | 2.0E-08 |
sp|B0U365|GLO2_XYLFM | Hydroxyacylglutathione hydrolase OS=Xylella fastidiosa (strain M12) GN=gloB PE=3 SV=1 | 92 | 203 | 2.0E-08 |
sp|Q46GM1|GLO2_PROMT | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain NATL2A) GN=gloB PE=3 SV=2 | 91 | 229 | 3.0E-08 |
sp|A2C116|GLO2_PROM1 | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain NATL1A) GN=gloB PE=3 SV=1 | 91 | 229 | 3.0E-08 |
sp|Q08889|GLO2_BUCAP | Hydroxyacylglutathione hydrolase OS=Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) GN=gloB PE=3 SV=1 | 87 | 190 | 3.0E-08 |
sp|A5ETG1|GLO2_BRASB | Hydroxyacylglutathione hydrolase OS=Bradyrhizobium sp. (strain BTAi1 / ATCC BAA-1182) GN=gloB PE=3 SV=1 | 76 | 190 | 8.0E-08 |
sp|Q3J436|GLO2_RHOS4 | Hydroxyacylglutathione hydrolase OS=Rhodobacter sphaeroides (strain ATCC 17023 / 2.4.1 / NCIB 8253 / DSM 158) GN=gloB PE=3 SV=1 | 72 | 186 | 8.0E-08 |
sp|A1RK78|GLO2_SHESW | Hydroxyacylglutathione hydrolase OS=Shewanella sp. (strain W3-18-1) GN=gloB PE=3 SV=1 | 84 | 187 | 9.0E-08 |
sp|Q4FP49|GLO2_PELUB | Hydroxyacylglutathione hydrolase OS=Pelagibacter ubique (strain HTCC1062) GN=gloB PE=3 SV=1 | 56 | 190 | 9.0E-08 |
sp|A4SPI6|GLO2_AERS4 | Hydroxyacylglutathione hydrolase OS=Aeromonas salmonicida (strain A449) GN=gloB PE=3 SV=1 | 91 | 187 | 9.0E-08 |
sp|A3PIB4|GLO2_RHOS1 | Hydroxyacylglutathione hydrolase OS=Rhodobacter sphaeroides (strain ATCC 17029 / ATH 2.4.9) GN=gloB PE=3 SV=1 | 90 | 186 | 1.0E-07 |
sp|Q28333|GLO2_CALJA | Hydroxyacylglutathione hydrolase, mitochondrial (Fragment) OS=Callithrix jacchus GN=HAGH PE=2 SV=2 | 72 | 203 | 1.0E-07 |
sp|Q92MF8|GLO2_RHIME | Hydroxyacylglutathione hydrolase OS=Rhizobium meliloti (strain 1021) GN=gloB PE=3 SV=1 | 70 | 186 | 1.0E-07 |
sp|Q7VM19|GLO2_HAEDU | Hydroxyacylglutathione hydrolase OS=Haemophilus ducreyi (strain 35000HP / ATCC 700724) GN=gloB PE=3 SV=1 | 57 | 222 | 1.0E-07 |
sp|B8F6A3|GLO2_HAEPS | Hydroxyacylglutathione hydrolase OS=Haemophilus parasuis serovar 5 (strain SH0165) GN=gloB PE=3 SV=1 | 57 | 205 | 1.0E-07 |
sp|A2BQ40|GLO2_PROMS | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain AS9601) GN=gloB PE=3 SV=2 | 45 | 222 | 1.0E-07 |
sp|Q8N490|PNKD_HUMAN | Probable hydrolase PNKD OS=Homo sapiens GN=PNKD PE=1 SV=2 | 72 | 254 | 1.0E-07 |
sp|Q7VQB7|GLO2_BLOFL | Hydroxyacylglutathione hydrolase OS=Blochmannia floridanus GN=gloB PE=3 SV=1 | 100 | 227 | 1.0E-07 |
sp|Q5ZVZ3|GLO2_LEGPH | Hydroxyacylglutathione hydrolase OS=Legionella pneumophila subsp. pneumophila (strain Philadelphia 1 / ATCC 33152 / DSM 7513) GN=gloB PE=3 SV=1 | 92 | 192 | 2.0E-07 |
sp|Q69ZP3|PNKD_MOUSE | Probable hydrolase PNKD OS=Mus musculus GN=Pnkd PE=1 SV=2 | 72 | 254 | 2.0E-07 |
sp|A5IBE7|GLO2_LEGPC | Hydroxyacylglutathione hydrolase OS=Legionella pneumophila (strain Corby) GN=gloB PE=3 SV=1 | 92 | 192 | 2.0E-07 |
sp|Q5WX41|GLO2_LEGPL | Hydroxyacylglutathione hydrolase OS=Legionella pneumophila (strain Lens) GN=gloB PE=3 SV=1 | 92 | 192 | 2.0E-07 |
sp|Q3BWP5|GLO2_XANC5 | Hydroxyacylglutathione hydrolase OS=Xanthomonas campestris pv. vesicatoria (strain 85-10) GN=gloB PE=3 SV=1 | 84 | 187 | 2.0E-07 |
sp|A1S6T3|GLO2_SHEAM | Hydroxyacylglutathione hydrolase OS=Shewanella amazonensis (strain ATCC BAA-1098 / SB2B) GN=gloB PE=3 SV=1 | 84 | 229 | 3.0E-07 |
sp|A4Y6B8|GLO2_SHEPC | Hydroxyacylglutathione hydrolase OS=Shewanella putrefaciens (strain CN-32 / ATCC BAA-453) GN=gloB PE=3 SV=1 | 84 | 187 | 3.0E-07 |
sp|Q5X5R2|GLO2_LEGPA | Hydroxyacylglutathione hydrolase OS=Legionella pneumophila (strain Paris) GN=gloB PE=3 SV=1 | 92 | 192 | 4.0E-07 |
sp|A1U0V1|GLO2_MARHV | Hydroxyacylglutathione hydrolase OS=Marinobacter hydrocarbonoclasticus (strain ATCC 700491 / DSM 11845 / VT8) GN=gloB PE=3 SV=1 | 84 | 187 | 5.0E-07 |
sp|B1WUT9|GLO2_CYAA5 | Hydroxyacylglutathione hydrolase OS=Cyanothece sp. (strain ATCC 51142) GN=gloB PE=3 SV=1 | 80 | 255 | 6.0E-07 |
sp|Q31BX5|GLO2_PROM9 | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain MIT 9312) GN=gloB PE=3 SV=1 | 91 | 222 | 8.0E-07 |
sp|B7VIP5|GLO2_VIBTL | Hydroxyacylglutathione hydrolase OS=Vibrio tasmaniensis (strain LGP32) GN=gloB PE=3 SV=1 | 91 | 192 | 9.0E-07 |
sp|A9BEI3|GLO2_PROM4 | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain MIT 9211) GN=gloB PE=3 SV=1 | 57 | 186 | 1.0E-06 |
sp|Q3AYI2|GLO2_SYNS9 | Hydroxyacylglutathione hydrolase OS=Synechococcus sp. (strain CC9902) GN=gloB PE=3 SV=1 | 57 | 187 | 1.0E-06 |
sp|C4K7Z9|GLO2_HAMD5 | Hydroxyacylglutathione hydrolase OS=Hamiltonella defensa subsp. Acyrthosiphon pisum (strain 5AT) GN=gloB PE=3 SV=1 | 57 | 187 | 1.0E-06 |
sp|A6WMW5|GLO2_SHEB8 | Hydroxyacylglutathione hydrolase OS=Shewanella baltica (strain OS185) GN=gloB PE=3 SV=1 | 37 | 186 | 1.0E-06 |
sp|A3MZD3|GLO2_ACTP2 | Hydroxyacylglutathione hydrolase OS=Actinobacillus pleuropneumoniae serotype 5b (strain L20) GN=gloB PE=3 SV=1 | 72 | 222 | 1.0E-06 |
sp|A2C7W3|GLO2_PROM3 | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain MIT 9303) GN=gloB PE=3 SV=1 | 57 | 186 | 2.0E-06 |
sp|A7Z4X7|BAEB_BACMF | Probable polyketide biosynthesis zinc-dependent hydrolase BaeB OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeB PE=1 SV=1 | 87 | 216 | 2.0E-06 |
sp|Q6D1V5|GLO2_PECAS | Hydroxyacylglutathione hydrolase OS=Pectobacterium atrosepticum (strain SCRI 1043 / ATCC BAA-672) GN=gloB PE=3 SV=1 | 57 | 187 | 2.0E-06 |
sp|Q7U5Z8|GLO2_SYNPX | Hydroxyacylglutathione hydrolase OS=Synechococcus sp. (strain WH8102) GN=gloB PE=3 SV=1 | 56 | 187 | 2.0E-06 |
sp|A3D437|GLO2_SHEB5 | Hydroxyacylglutathione hydrolase OS=Shewanella baltica (strain OS155 / ATCC BAA-1091) GN=gloB PE=3 SV=1 | 37 | 186 | 2.0E-06 |
sp|Q2P6Y4|GLO2_XANOM | Hydroxyacylglutathione hydrolase OS=Xanthomonas oryzae pv. oryzae (strain MAFF 311018) GN=gloB PE=3 SV=1 | 64 | 187 | 2.0E-06 |
sp|Q2JPX4|GLO2_SYNJB | Hydroxyacylglutathione hydrolase OS=Synechococcus sp. (strain JA-2-3B'a(2-13)) GN=gloB PE=3 SV=1 | 80 | 187 | 2.0E-06 |
sp|A4G7G5|GLO2_HERAR | Hydroxyacylglutathione hydrolase OS=Herminiimonas arsenicoxydans GN=gloB PE=3 SV=1 | 63 | 187 | 3.0E-06 |
sp|Q5LNN5|GLO2_RUEPO | Hydroxyacylglutathione hydrolase OS=Ruegeria pomeroyi (strain ATCC 700808 / DSM 15171 / DSS-3) GN=gloB PE=3 SV=1 | 72 | 186 | 3.0E-06 |
sp|Q8PNI0|GLO2_XANAC | Hydroxyacylglutathione hydrolase OS=Xanthomonas axonopodis pv. citri (strain 306) GN=gloB PE=3 SV=1 | 64 | 187 | 3.0E-06 |
sp|Q5QZL0|GLO2_IDILO | Hydroxyacylglutathione hydrolase OS=Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) GN=gloB PE=3 SV=1 | 63 | 257 | 3.0E-06 |
sp|Q46Z82|GLO2_CUPPJ | Hydroxyacylglutathione hydrolase OS=Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) GN=gloB PE=3 SV=1 | 57 | 288 | 4.0E-06 |
sp|B8E5A2|GLO2_SHEB2 | Hydroxyacylglutathione hydrolase OS=Shewanella baltica (strain OS223) GN=gloB PE=3 SV=1 | 37 | 186 | 5.0E-06 |
sp|Q1LL91|GLO2_CUPMC | Hydroxyacylglutathione hydrolase OS=Cupriavidus metallidurans (strain ATCC 43123 / DSM 2839 / NBRC 102507 / CH34) GN=gloB PE=3 SV=1 | 57 | 187 | 5.0E-06 |
sp|A3PBT3|GLO2_PROM0 | Hydroxyacylglutathione hydrolase OS=Prochlorococcus marinus (strain MIT 9301) GN=gloB PE=3 SV=2 | 91 | 205 | 5.0E-06 |
sp|A1WXD9|GLO2_HALHL | Hydroxyacylglutathione hydrolase OS=Halorhodospira halophila (strain DSM 244 / SL1) GN=gloB PE=3 SV=1 | 84 | 206 | 6.0E-06 |
sp|Q8DBD8|GLO2_VIBVU | Hydroxyacylglutathione hydrolase OS=Vibrio vulnificus (strain CMCP6) GN=gloB PE=3 SV=1 | 84 | 190 | 6.0E-06 |
sp|Q7MII4|GLO22_VIBVY | Hydroxyacylglutathione hydrolase 2 OS=Vibrio vulnificus (strain YJ016) GN=gloB2 PE=3 SV=1 | 84 | 190 | 6.0E-06 |
sp|Q3AL08|GLO2_SYNSC | Hydroxyacylglutathione hydrolase OS=Synechococcus sp. (strain CC9605) GN=gloB PE=3 SV=1 | 56 | 187 | 7.0E-06 |
sp|A9L0E9|GLO2_SHEB9 | Hydroxyacylglutathione hydrolase OS=Shewanella baltica (strain OS195) GN=gloB PE=3 SV=1 | 37 | 187 | 9.0E-06 |
sp|B0JW10|GLO2_MICAN | Hydroxyacylglutathione hydrolase OS=Microcystis aeruginosa (strain NIES-843) GN=gloB PE=3 SV=1 | 91 | 205 | 9.0E-06 |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 27 | 0.45 |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
Protein | >Hirsu2|5820 MKEDKGGYRQINKALNVCAFEDYLEGQRARLPPLANVEQLTPRVLRVLGQNPGKFTLQGTNTYIVGTGPQRLIID TSGGEAAWAQLLASALESRGIELSAVLLTHWHGDHTGGVPDLVRLYPHLRDSIFKNEPGPEQRDVAEGQVFQVDG ATVRALHAPGHSDDHMCFVLEEEQAMFTGDNVLGHGSSAVQDLGAFMASLGRMRSQGCVVGYPAHGAAVADLPAK IAGELEIKWRRERQVLQALARARAREDRSVGLSDLVTDMYGAPLDEEVRTLALEPFVDEVLRKLAGDGSVAFEMR GGKRKWYSVETV* |
Coding | >Hirsu2|5820 ATGAAAGAAGACAAGGGCGGCTACCGCCAGATCAACAAAGCGTTGAACGTCTGCGCGTTCGAAGACTACCTCGAA GGCCAGAGAGCACGACTGCCGCCGCTCGCCAACGTTGAGCAGCTCACCCCCAGGGTGCTGCGCGTGCTCGGCCAG AATCCAGGCAAGTTCACCTTGCAGGGGACCAACACGTATATCGTCGGCACTGGGCCCCAGCGGCTCATCATCGAC ACGTCCGGCGGCGAGGCGGCCTGGGCCCAACTTCTTGCGTCCGCACTCGAGTCGAGAGGCATCGAGCTGTCGGCC GTGCTGCTGACGCACTGGCACGGCGATCACACCGGCGGCGTCCCCGACCTCGTCCGCCTGTACCCGCACCTCCGG GACTCCATCTTCAAGAACGAGCCGGGCCCGGAGCAGCGGGACGTGGCCGAAGGGCAGGTCTTCCAGGTCGACGGC GCCACCGTCCGCGCCCTGCACGCCCCGGGCCACTCGGATGACCACATGTGCTTCGTCCTCGAGGAGGAGCAGGCC ATGTTCACCGGCGACAACGTTCTCGGCCACGGCAGCAGCGCGGTCCAGGACCTCGGTGCCTTCATGGCGAGCCTG GGGCGCATGCGATCGCAGGGGTGCGTGGTCGGCTATCCCGCCCACGGCGCCGCCGTCGCCGACCTGCCGGCGAAG ATCGCCGGCGAGCTGGAGATCAAGTGGCGCCGCGAGCGCCAGGTCCTGCAGGCCCTCGCCCGCGCCCGCGCCCGC GAGGATCGGAGCGTCGGCCTCAGCGACCTTGTGACTGACATGTACGGCGCGCCGCTGGACGAGGAGGTGCGCACG CTCGCGCTGGAACCCTTTGTCGACGAAGTGCTGCGGAAGCTGGCGGGCGACGGCAGCGTCGCCTTCGAAATGAGA GGCGGTAAAAGGAAATGGTACTCAGTCGAGACAGTATAG |
Transcript | >Hirsu2|5820 ATGAAAGAAGACAAGGGCGGCTACCGCCAGATCAACAAAGCGTTGAACGTCTGCGCGTTCGAAGACTACCTCGAA GGCCAGAGAGCACGACTGCCGCCGCTCGCCAACGTTGAGCAGCTCACCCCCAGGGTGCTGCGCGTGCTCGGCCAG AATCCAGGCAAGTTCACCTTGCAGGGGACCAACACGTATATCGTCGGCACTGGGCCCCAGCGGCTCATCATCGAC ACGTCCGGCGGCGAGGCGGCCTGGGCCCAACTTCTTGCGTCCGCACTCGAGTCGAGAGGCATCGAGCTGTCGGCC GTGCTGCTGACGCACTGGCACGGCGATCACACCGGCGGCGTCCCCGACCTCGTCCGCCTGTACCCGCACCTCCGG GACTCCATCTTCAAGAACGAGCCGGGCCCGGAGCAGCGGGACGTGGCCGAAGGGCAGGTCTTCCAGGTCGACGGC GCCACCGTCCGCGCCCTGCACGCCCCGGGCCACTCGGATGACCACATGTGCTTCGTCCTCGAGGAGGAGCAGGCC ATGTTCACCGGCGACAACGTTCTCGGCCACGGCAGCAGCGCGGTCCAGGACCTCGGTGCCTTCATGGCGAGCCTG GGGCGCATGCGATCGCAGGGGTGCGTGGTCGGCTATCCCGCCCACGGCGCCGCCGTCGCCGACCTGCCGGCGAAG ATCGCCGGCGAGCTGGAGATCAAGTGGCGCCGCGAGCGCCAGGTCCTGCAGGCCCTCGCCCGCGCCCGCGCCCGC GAGGATCGGAGCGTCGGCCTCAGCGACCTTGTGACTGACATGTACGGCGCGCCGCTGGACGAGGAGGTGCGCACG CTCGCGCTGGAACCCTTTGTCGACGAAGTGCTGCGGAAGCTGGCGGGCGACGGCAGCGTCGCCTTCGAAATGAGA GGCGGTAAAAGGAAATGGTACTCAGTCGAGACAGTATAG |
Gene | >Hirsu2|5820 ATGAAAGAAGACAAGGGCGGCTACCGCCAGATCAACAAAGCGTTGAACGTCTGCGCGTTCGAAGACTACCTCGAA GGCCAGAGAGCACGACTGCCGCCGCTCGCCAACGTTGAGCAGCTCACCCCCAGGGTGCTGCGCGTGCTCGGCCAG AATCCAGGCAAGGTAGAGTGGGCGTCACGGCCGACTGGCAGAGCGAGCAAACGCCATGGCTGATCACCGTGCGCT GCCCAGTTCACCTTGCAGGGGACCAACACGTATATCGTCGGCACTGGGCCCCAGCGGCTCATCATCGACACGTCC GGCGGCGAGGCGGCCTGGGCCCAACTTCTTGCGTCCGCACTCGAGTCGAGAGGCATCGAGCTGTCGGCCGTGCTG CTGACGCACTGGCACGGCGATCACACCGGCGGCGTCCCCGACCTCGTCCGCCTGTACCCGCACCTCCGGGACTCC ATCTTCAAGAACGAGCCGGGCCCGGAGCAGCGGGACGTGGCCGAAGGGCAGGTCTTCCAGGTCGACGGCGCCACC GTCCGCGCCCTGCACGCCCCGGGCCACTCGGATGACCACATGTGCTTCGTCCTCGAGGAGGAGCAGGCCATGTTC ACCGGCGACAACGTTCTCGGCCACGGCAGCAGCGCGGTCCAGGACCTCGGTGCCTTCATGGCGAGCCTGGGGCGC ATGCGATCGCAGGGGTGCGTGGTCGGCTATCCCGCCCACGGCGCCGCCGTCGCCGACCTGCCGGCGAAGATCGCC GGCGAGCTGGAGATCAAGTGGCGCCGCGAGCGCCAGGTCCTGCAGGCCCTCGCCCGCGCCCGCGCCCGCGAGGAT CGGAGCGTCGGCCTCAGCGACCTTGTGACTGACATGTACGGCGCGCCGCTGGACGAGGAGGTGCGCACGCTCGCG CTGGAACCCTTTGTCGACGAAGTGCTGCGGAAGCTGGCGGGCGACGGCAGCGTCGCCTTCGAAATGAGAGGCGGT AAAAGGAAATGGTACTCAGTCGAGACAGTATAG |