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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QG77
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 248 | 252 | PF00656 | 0.674 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.560 |
CLV_PCSK_FUR_1 | 356 | 360 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.570 |
CLV_PCSK_PC7_1 | 62 | 68 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.578 |
DEG_APCC_DBOX_1 | 109 | 117 | PF00400 | 0.555 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.586 |
DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.534 |
DOC_CKS1_1 | 360 | 365 | PF01111 | 0.424 |
DOC_CKS1_1 | 542 | 547 | PF01111 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 445 | 451 | PF00134 | 0.689 |
DOC_CYCLIN_yCln2_LP_2 | 462 | 468 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 542 | 548 | PF00134 | 0.560 |
DOC_MAPK_gen_1 | 519 | 528 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 62 | 71 | PF00069 | 0.536 |
DOC_MAPK_HePTP_8 | 516 | 528 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 519 | 528 | PF00069 | 0.424 |
DOC_MAPK_RevD_3 | 52 | 67 | PF00069 | 0.485 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.505 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.615 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 228 | 232 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 417 | 422 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 495 | 505 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 82 | 89 | PF00244 | 0.652 |
LIG_Actin_WH2_2 | 264 | 282 | PF00022 | 0.493 |
LIG_Actin_WH2_2 | 420 | 438 | PF00022 | 0.427 |
LIG_Actin_WH2_2 | 480 | 497 | PF00022 | 0.467 |
LIG_APCC_ABBA_1 | 342 | 347 | PF00400 | 0.415 |
LIG_Clathr_ClatBox_1 | 484 | 488 | PF01394 | 0.364 |
LIG_Clathr_ClatBox_1 | 539 | 543 | PF01394 | 0.405 |
LIG_CSL_BTD_1 | 145 | 148 | PF09270 | 0.666 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.645 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.468 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.454 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.454 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.507 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.466 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.450 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.473 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.529 |
LIG_GBD_Chelix_1 | 285 | 293 | PF00786 | 0.435 |
LIG_LIR_Gen_1 | 105 | 116 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 534 | 539 | PF02991 | 0.369 |
LIG_NRBOX | 288 | 294 | PF00104 | 0.513 |
LIG_NRBOX | 53 | 59 | PF00104 | 0.538 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 162 | 165 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.431 |
LIG_SH3_2 | 545 | 550 | PF14604 | 0.593 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.622 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.587 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.492 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.642 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.369 |
LIG_SH3_3 | 542 | 548 | PF00018 | 0.608 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.619 |
LIG_SUMO_SIM_anti_2 | 418 | 423 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 207 | 214 | PF11976 | 0.447 |
LIG_TYR_ITIM | 484 | 489 | PF00017 | 0.362 |
LIG_UBA3_1 | 70 | 75 | PF00899 | 0.568 |
LIG_WW_3 | 79 | 83 | PF00397 | 0.626 |
MOD_CDC14_SPxK_1 | 547 | 550 | PF00782 | 0.601 |
MOD_CDK_SPxK_1 | 544 | 550 | PF00069 | 0.586 |
MOD_CDK_SPxxK_3 | 410 | 417 | PF00069 | 0.523 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.608 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.692 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.649 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.630 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.640 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.495 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.481 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.500 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.617 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.500 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.572 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.651 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.606 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.636 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.524 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.716 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.648 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.552 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.615 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.477 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.680 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.667 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.535 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.650 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.523 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.641 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.613 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.406 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.654 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.604 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.533 |
MOD_N-GLC_2 | 525 | 527 | PF02516 | 0.439 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.583 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.557 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.653 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.423 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.422 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.518 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.569 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.587 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.596 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.475 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.516 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.590 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.581 |
MOD_PK_1 | 477 | 483 | PF00069 | 0.370 |
MOD_PKA_1 | 358 | 364 | PF00069 | 0.465 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.534 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.567 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.514 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.705 |
MOD_PKB_1 | 356 | 364 | PF00069 | 0.466 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.409 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.647 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.552 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.370 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.411 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.738 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.527 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.528 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.583 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.544 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.489 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.433 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.682 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.550 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.384 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.595 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.466 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.644 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.725 |
TRG_DiLeu_BaEn_1 | 426 | 431 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.378 |
TRG_NLS_MonoExtN_4 | 62 | 69 | PF00514 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 537 | 541 | PF00026 | 0.380 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEI5 | Leptomonas seymouri | 32% | 93% |
A0A3S7WSG2 | Leishmania donovani | 90% | 100% |
A4H766 | Leishmania braziliensis | 68% | 99% |
A4HVK5 | Leishmania infantum | 90% | 100% |
E9APA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |