Carbonic anhydrase protein (luminal). Based on its distant eukaryotic relatives, it probably has a signal peptide on its N-terminus and a membrane anchor at the C-terminus
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. | no | yes: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 6, no: 0 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HG87
Term | Name | Level | Count |
---|---|---|---|
GO:0006730 | one-carbon metabolic process | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004089 | carbonate dehydratase activity | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016829 | lyase activity | 2 | 7 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 7 |
GO:0016836 | hydro-lyase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.312 |
CLV_C14_Caspase3-7 | 422 | 426 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.422 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.484 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.668 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.207 |
DEG_SCF_TRCP1_1 | 378 | 383 | PF00400 | 0.424 |
DEG_SPOP_SBC_1 | 198 | 202 | PF00917 | 0.246 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.429 |
DEG_SPOP_SBC_1 | 482 | 486 | PF00917 | 0.526 |
DOC_CYCLIN_yCln2_LP_2 | 390 | 396 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 165 | 175 | PF00069 | 0.209 |
DOC_MAPK_gen_1 | 183 | 192 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 573 | 581 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 168 | 177 | PF00069 | 0.251 |
DOC_MAPK_MEF2A_6 | 185 | 194 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 548 | 556 | PF00069 | 0.253 |
DOC_PP1_RVXF_1 | 93 | 99 | PF00149 | 0.271 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.264 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.207 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.286 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.207 |
LIG_14-3-3_CanoR_1 | 222 | 230 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 275 | 279 | PF00244 | 0.207 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.207 |
LIG_14-3-3_CanoR_1 | 389 | 393 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 553 | 559 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 95 | 105 | PF00244 | 0.248 |
LIG_14-3-3_CterR_2 | 611 | 615 | PF00244 | 0.592 |
LIG_Actin_WH2_2 | 269 | 284 | PF00022 | 0.207 |
LIG_BIR_III_4 | 397 | 401 | PF00653 | 0.428 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.205 |
LIG_eIF4E_1 | 39 | 45 | PF01652 | 0.448 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.444 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.246 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.301 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.298 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.373 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.216 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.429 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.404 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.438 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.487 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.680 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.296 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.207 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 526 | 537 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 55 | 65 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 78 | 87 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 515 | 520 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 595 | 601 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.281 |
LIG_PDZ_Class_1 | 610 | 615 | PF00595 | 0.591 |
LIG_Pex14_2 | 531 | 535 | PF04695 | 0.306 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.383 |
LIG_SH2_GRB2like | 58 | 61 | PF00017 | 0.334 |
LIG_SH2_NCK_1 | 546 | 550 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.675 |
LIG_SH3_2 | 495 | 500 | PF14604 | 0.440 |
LIG_SH3_2 | 606 | 611 | PF14604 | 0.583 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.312 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.441 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.493 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.644 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.585 |
LIG_SUMO_SIM_anti_2 | 191 | 196 | PF11976 | 0.205 |
LIG_SUMO_SIM_par_1 | 391 | 397 | PF11976 | 0.425 |
LIG_WRC_WIRS_1 | 532 | 537 | PF05994 | 0.302 |
MOD_CDK_SPxxK_3 | 520 | 527 | PF00069 | 0.346 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.233 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.239 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.268 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.262 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.258 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.267 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.426 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.507 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.548 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.455 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.475 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.574 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.505 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.491 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.513 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.379 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.395 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.290 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.207 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.496 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.425 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.610 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.628 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.651 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.726 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.783 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.718 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.649 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.644 |
MOD_GlcNHglycan | 470 | 474 | PF01048 | 0.734 |
MOD_GlcNHglycan | 50 | 54 | PF01048 | 0.644 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.639 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.451 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.296 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.275 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.414 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.473 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.516 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.593 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.630 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.449 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.448 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.571 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.527 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.468 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.321 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.468 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.468 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.676 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.677 |
MOD_N-GLC_1 | 459 | 464 | PF02516 | 0.703 |
MOD_N-GLC_1 | 477 | 482 | PF02516 | 0.642 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.701 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.268 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.568 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.268 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.271 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.293 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.358 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.492 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.304 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.248 |
MOD_NEK2_2 | 224 | 229 | PF00069 | 0.268 |
MOD_NEK2_2 | 384 | 389 | PF00069 | 0.525 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.296 |
MOD_PK_1 | 533 | 539 | PF00069 | 0.361 |
MOD_PKA_1 | 337 | 343 | PF00069 | 0.413 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.207 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.281 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.207 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.589 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.448 |
MOD_PKB_1 | 346 | 354 | PF00069 | 0.426 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.295 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.234 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.380 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.405 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.283 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.306 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.234 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.207 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.304 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.528 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.552 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.431 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.286 |
MOD_SUMO_rev_2 | 477 | 482 | PF00179 | 0.435 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.683 |
TRG_NLS_Bipartite_1 | 324 | 340 | PF00514 | 0.399 |
TRG_NLS_MonoCore_2 | 334 | 339 | PF00514 | 0.404 |
TRG_NLS_MonoExtN_4 | 324 | 329 | PF00514 | 0.408 |
TRG_NLS_MonoExtN_4 | 335 | 340 | PF00514 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 165 | 170 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBI8 | Leptomonas seymouri | 49% | 97% |
A0A3Q8IDR5 | Leishmania donovani | 61% | 98% |
A4I3A0 | Leishmania infantum | 61% | 98% |
E9AZK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
Q4Q8M3 | Leishmania major | 59% | 100% |