Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 3 |
NetGPI | no | yes: 0, no: 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HY21
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
GO:0120029 | proton export across plasma membrane | 4 | 1 |
GO:0140115 | export across plasma membrane | 3 | 1 |
GO:0140352 | export from cell | 2 | 1 |
GO:1902600 | proton transmembrane transport | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 4 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0005524 | ATP binding | 5 | 4 |
GO:0016462 | pyrophosphatase activity | 5 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 4 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 4 |
GO:0016887 | ATP hydrolysis activity | 7 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 4 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 4 |
GO:0032553 | ribonucleotide binding | 3 | 4 |
GO:0032555 | purine ribonucleotide binding | 4 | 4 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 4 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 4 |
GO:0036094 | small molecule binding | 2 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:0097367 | carbohydrate derivative binding | 2 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
GO:0005215 | transporter activity | 1 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0008553 | P-type proton-exporting transporter activity | 4 | 1 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015078 | proton transmembrane transporter activity | 5 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 1 |
GO:0015662 | P-type ion transporter activity | 4 | 1 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 1 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 1 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.185 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.342 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.185 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.214 |
CLV_Separin_Metazoa | 391 | 395 | PF03568 | 0.510 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.570 |
DEG_SCF_SKP2-CKS1_1 | 22 | 29 | PF00560 | 0.618 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.408 |
DOC_ANK_TNKS_1 | 224 | 231 | PF00023 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 55 | 58 | PF00134 | 0.547 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.223 |
DOC_MAPK_gen_1 | 263 | 269 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 445 | 454 | PF00069 | 0.441 |
DOC_PP2B_LxvP_1 | 500 | 503 | PF13499 | 0.461 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.547 |
DOC_PP4_FxxP_1 | 499 | 502 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 147 | 151 | PF12436 | 0.533 |
DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.414 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.408 |
LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 478 | 483 | PF00244 | 0.433 |
LIG_14-3-3_CterR_2 | 512 | 514 | PF00244 | 0.543 |
LIG_Actin_WH2_2 | 248 | 265 | PF00022 | 0.385 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 113 | 122 | PF00928 | 0.185 |
LIG_EH1_1 | 297 | 305 | PF00400 | 0.408 |
LIG_EH1_1 | 448 | 456 | PF00400 | 0.446 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.414 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.509 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.431 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.505 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.483 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.448 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.478 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.555 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.489 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.633 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.498 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.576 |
LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.232 |
LIG_LIR_Apic_2 | 498 | 502 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 159 | 170 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.467 |
LIG_NBox_RRM_1 | 292 | 302 | PF00076 | 0.414 |
LIG_PCNA_PIPBox_1 | 493 | 502 | PF02747 | 0.438 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.414 |
LIG_REV1ctd_RIR_1 | 238 | 247 | PF16727 | 0.408 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.650 |
LIG_SH2_STAP1 | 6 | 10 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.232 |
LIG_SH3_2 | 27 | 32 | PF14604 | 0.629 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.385 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.625 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.408 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.499 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.466 |
LIG_SUMO_SIM_anti_2 | 463 | 471 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 192 | 199 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 300 | 306 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 307 | 312 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 316 | 323 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 463 | 471 | PF11976 | 0.450 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.495 |
LIG_TRAF2_1 | 63 | 66 | PF00917 | 0.491 |
LIG_WRC_WIRS_1 | 289 | 294 | PF05994 | 0.414 |
LIG_WRC_WIRS_1 | 496 | 501 | PF05994 | 0.440 |
LIG_WW_3 | 391 | 395 | PF00397 | 0.510 |
LIG_WW_3 | 501 | 505 | PF00397 | 0.473 |
MOD_CDK_SPxK_1 | 23 | 29 | PF00069 | 0.617 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.433 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.581 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.487 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.616 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.408 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.474 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.485 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.491 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.281 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.302 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.328 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.282 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.532 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.550 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.408 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.408 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.577 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.463 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.577 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.707 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.435 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.515 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.544 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.223 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.540 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.427 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.481 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.389 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.452 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.452 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.344 |
MOD_NEK2_2 | 152 | 157 | PF00069 | 0.372 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.408 |
MOD_PK_1 | 32 | 38 | PF00069 | 0.597 |
MOD_PK_1 | 478 | 484 | PF00069 | 0.437 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.597 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.441 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.597 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.508 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.594 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.223 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.408 |
MOD_Plk_2-3 | 18 | 24 | PF00069 | 0.616 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.443 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.561 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.597 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.595 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.527 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.454 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.439 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.532 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.633 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.408 |
MOD_SUMO_rev_2 | 371 | 379 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 501 | 510 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 78 | 85 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 9 | 17 | PF00179 | 0.625 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_4 | 371 | 377 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IUN3 | Bodo saltans | 72% | 69% |
A0RA13 | Bacillus thuringiensis (strain Al Hakam) | 25% | 74% |
A4H9S2 | Leishmania braziliensis | 90% | 100% |
A7FFQ9 | Yersinia pseudotuberculosis serotype O:1b (strain IP 31758) | 26% | 75% |
A7GLG4 | Bacillus cytotoxicus (strain DSM 22905 / CIP 110041 / 391-98 / NVH 391-98) | 25% | 74% |
A7ZJ80 | Escherichia coli O139:H28 (strain E24377A / ETEC) | 26% | 75% |
A8GB61 | Serratia proteamaculans (strain 568) | 26% | 75% |
A9VFM1 | Bacillus mycoides (strain KBAB4) | 25% | 74% |
B0R9M0 | Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) | 21% | 71% |
B1IY32 | Escherichia coli (strain ATCC 8739 / DSM 1576 / NBRC 3972 / NCIMB 8545 / WDCM 00012 / Crooks) | 26% | 75% |
B1JR96 | Yersinia pseudotuberculosis serotype O:3 (strain YPIII) | 26% | 75% |
B1LLE1 | Escherichia coli (strain SMS-3-5 / SECEC) | 26% | 75% |
B1X6M8 | Escherichia coli (strain K12 / DH10B) | 26% | 75% |
B2TMJ2 | Clostridium botulinum (strain Eklund 17B / Type B) | 24% | 75% |
B2TTJ7 | Shigella boydii serotype 18 (strain CDC 3083-94 / BS512) | 27% | 75% |
B2V2P3 | Clostridium botulinum (strain Alaska E43 / Type E3) | 24% | 75% |
B5XZE9 | Klebsiella pneumoniae (strain 342) | 25% | 75% |
B5YQN9 | Escherichia coli O157:H7 (strain EC4115 / EHEC) | 26% | 75% |
B6HYQ5 | Escherichia coli (strain SE11) | 26% | 75% |
B7HDF9 | Bacillus cereus (strain B4264) | 25% | 74% |
B7HWG1 | Bacillus cereus (strain AH187) | 25% | 74% |
B7II09 | Bacillus cereus (strain G9842) | 26% | 74% |
B7JRB8 | Bacillus cereus (strain AH820) | 24% | 74% |
B7LAA4 | Escherichia coli (strain 55989 / EAEC) | 26% | 75% |
B7LKR7 | Escherichia fergusonii (strain ATCC 35469 / DSM 13698 / CCUG 18766 / IAM 14443 / JCM 21226 / LMG 7866 / NBRC 102419 / NCTC 12128 / CDC 0568-73) | 26% | 75% |
B7M5L3 | Escherichia coli O8 (strain IAI1) | 26% | 75% |
B7N9U0 | Escherichia coli O17:K52:H18 (strain UMN026 / ExPEC) | 27% | 75% |
B7NMQ0 | Escherichia coli O7:K1 (strain IAI39 / ExPEC) | 27% | 75% |
C1EYK0 | Bacillus cereus (strain 03BB102) | 25% | 74% |
C3LF99 | Bacillus anthracis (strain CDC 684 / NRRL 3495) | 25% | 74% |
C4LDL7 | Tolumonas auensis (strain DSM 9187 / TA4) | 25% | 75% |
C4ZWH3 | Escherichia coli (strain K12 / MC4100 / BW2952) | 26% | 75% |
O30085 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 23% | 74% |
P03960 | Escherichia coli (strain K12) | 26% | 75% |
P32113 | Enterococcus hirae (strain ATCC 9790 / DSM 20160 / JCM 8729 / LMG 6399 / NBRC 3181 / NCIMB 6459 / NCDO 1258 / NCTC 12367 / WDCM 00089 / R) | 22% | 71% |
P35597 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 24% | 66% |
P57699 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 21% | 71% |
P57700 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 22% | 77% |
P59219 | Leptospira interrogans serogroup Icterohaemorrhagiae serovar Lai (strain 56601) | 25% | 74% |
Q0TRT3 | Clostridium perfringens (strain ATCC 13124 / DSM 756 / JCM 1290 / NCIMB 6125 / NCTC 8237 / Type A) | 22% | 75% |
Q324L0 | Shigella boydii serotype 4 (strain Sb227) | 27% | 75% |
Q3Z4A6 | Shigella sonnei (strain Ss046) | 27% | 75% |
Q63FR0 | Bacillus cereus (strain ZK / E33L) | 25% | 74% |
Q667S4 | Yersinia pseudotuberculosis serotype I (strain IP32953) | 26% | 75% |
Q6HN78 | Bacillus thuringiensis subsp. konkukian (strain 97-27) | 24% | 74% |
Q72TM6 | Leptospira interrogans serogroup Icterohaemorrhagiae serovar copenhageni (strain Fiocruz L1-130) | 24% | 74% |
Q7N6W6 | Photorhabdus laumondii subsp. laumondii (strain DSM 15139 / CIP 105565 / TT01) | 24% | 75% |
Q81HQ0 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 25% | 74% |
Q8PCM1 | Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25) | 24% | 75% |
Q8X9F9 | Escherichia coli O157:H7 | 26% | 75% |
Q926K7 | Listeria innocua serovar 6a (strain ATCC BAA-680 / CLIP 11262) | 24% | 75% |
Q93MV5 | Myxococcus xanthus | 24% | 75% |
Q9CCL1 | Mycobacterium leprae (strain TN) | 21% | 71% |
Q9RZP0 | Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 / NBRC 15346 / NCIMB 9279 / R1 / VKM B-1422) | 24% | 76% |
Q9ZL53 | Helicobacter pylori (strain J99 / ATCC 700824) | 21% | 75% |