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: 0 |
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4IBP7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.681 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.673 |
CLV_PCSK_PC7_1 | 461 | 467 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.606 |
DOC_CYCLIN_RxL_1 | 224 | 235 | PF00134 | 0.552 |
DOC_MAPK_gen_1 | 123 | 131 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 435 | 443 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 82 | 88 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 286 | 295 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 380 | 389 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 522 | 530 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 550 | 557 | PF00149 | 0.418 |
DOC_PP2B_PxIxI_1 | 382 | 388 | PF00149 | 0.405 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.593 |
DOC_USP7_UBL2_3 | 338 | 342 | PF12436 | 0.405 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.569 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 123 | 129 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 13 | 21 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 143 | 148 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 202 | 209 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 477 | 486 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 489 | 498 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 539 | 547 | PF00244 | 0.410 |
LIG_Actin_WH2_2 | 423 | 440 | PF00022 | 0.260 |
LIG_BIR_III_2 | 206 | 210 | PF00653 | 0.553 |
LIG_Clathr_ClatBox_1 | 128 | 132 | PF01394 | 0.542 |
LIG_Clathr_ClatBox_1 | 352 | 356 | PF01394 | 0.380 |
LIG_DLG_GKlike_1 | 124 | 131 | PF00625 | 0.641 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.575 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.639 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.443 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.310 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.522 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.365 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.653 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.471 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.715 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.636 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.598 |
LIG_LIR_Gen_1 | 348 | 358 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 514 | 524 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.482 |
LIG_MYND_1 | 161 | 165 | PF01753 | 0.602 |
LIG_MYND_1 | 279 | 283 | PF01753 | 0.433 |
LIG_MYND_1 | 46 | 50 | PF01753 | 0.607 |
LIG_PCNA_TLS_4 | 344 | 351 | PF02747 | 0.405 |
LIG_PCNA_yPIPBox_3 | 438 | 452 | PF02747 | 0.405 |
LIG_PTB_Apo_2 | 271 | 278 | PF02174 | 0.507 |
LIG_RPA_C_Fungi | 119 | 131 | PF08784 | 0.557 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.602 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.545 |
LIG_SH2_CRK | 455 | 459 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.568 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.674 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.540 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.392 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.405 |
LIG_SUMO_SIM_anti_2 | 126 | 133 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 250 | 255 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 291 | 296 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 439 | 444 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 5 | 10 | PF11976 | 0.499 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.585 |
LIG_WRC_WIRS_1 | 546 | 551 | PF05994 | 0.444 |
MOD_CDC14_SPxK_1 | 164 | 167 | PF00782 | 0.635 |
MOD_CDC14_SPxK_1 | 224 | 227 | PF00782 | 0.517 |
MOD_CDK_SPK_2 | 197 | 202 | PF00069 | 0.578 |
MOD_CDK_SPxK_1 | 161 | 167 | PF00069 | 0.632 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.519 |
MOD_CDK_SPxxK_3 | 279 | 286 | PF00069 | 0.389 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.545 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.588 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.661 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.615 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.418 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.417 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.637 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.602 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.650 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.585 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.644 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.476 |
MOD_Cter_Amidation | 108 | 111 | PF01082 | 0.672 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.623 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.635 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.634 |
MOD_GlcNHglycan | 172 | 176 | PF01048 | 0.658 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.426 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.705 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.638 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.581 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.703 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.509 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.515 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.565 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.435 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.649 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.392 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.675 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.463 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.645 |
MOD_N-GLC_2 | 447 | 449 | PF02516 | 0.320 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.576 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.487 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.405 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.623 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.588 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.405 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.534 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.405 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.541 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.574 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.472 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.670 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.722 |
MOD_NEK2_2 | 454 | 459 | PF00069 | 0.344 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.408 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.580 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.507 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.415 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.601 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.597 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.655 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.563 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.621 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.485 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.405 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.405 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.507 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.415 |
MOD_PKB_1 | 114 | 122 | PF00069 | 0.618 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.405 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.607 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.478 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.685 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.601 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.556 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.612 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.405 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.322 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.263 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.478 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.449 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.632 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.522 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.544 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.603 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.468 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.374 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.344 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.613 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.569 |
MOD_SUMO_for_1 | 166 | 169 | PF00179 | 0.582 |
TRG_DiLeu_BaEn_1 | 523 | 528 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 54 | 59 | PF01217 | 0.585 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.465 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 376 | 381 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.645 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IIK2 | Leishmania donovani | 99% | 100% |
A4HN21 | Leishmania braziliensis | 59% | 90% |
E9AFH6 | Leishmania major | 88% | 100% |
E9B6N1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 98% |