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: E9APA1
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 | 249 | 253 | PF00656 | 0.687 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.455 |
CLV_PCSK_FUR_1 | 357 | 361 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.458 |
CLV_PCSK_PC7_1 | 62 | 68 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 110 | 118 | PF00400 | 0.535 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.559 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.534 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.408 |
DOC_CKS1_1 | 542 | 547 | PF01111 | 0.555 |
DOC_CYCLIN_RxL_1 | 62 | 73 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 445 | 451 | PF00134 | 0.579 |
DOC_CYCLIN_yCln2_LP_2 | 462 | 468 | PF00134 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 542 | 548 | PF00134 | 0.558 |
DOC_MAPK_gen_1 | 62 | 71 | PF00069 | 0.477 |
DOC_MAPK_HePTP_8 | 516 | 528 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 207 | 214 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 519 | 528 | PF00069 | 0.401 |
DOC_MAPK_RevD_3 | 52 | 67 | PF00069 | 0.406 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.455 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.639 |
DOC_USP7_MATH_2 | 304 | 310 | PF00917 | 0.493 |
DOC_USP7_UBL2_3 | 123 | 127 | PF12436 | 0.503 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.379 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 229 | 233 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 421 | 431 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 495 | 505 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 82 | 89 | PF00244 | 0.649 |
LIG_Actin_WH2_2 | 265 | 283 | PF00022 | 0.486 |
LIG_Actin_WH2_2 | 480 | 497 | PF00022 | 0.442 |
LIG_BIR_III_4 | 374 | 378 | PF00653 | 0.394 |
LIG_Clathr_ClatBox_1 | 484 | 488 | PF01394 | 0.346 |
LIG_Clathr_ClatBox_1 | 539 | 543 | PF01394 | 0.397 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.633 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.454 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.451 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.402 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.649 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.418 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.379 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.475 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.419 |
LIG_GBD_Chelix_1 | 286 | 294 | PF00786 | 0.435 |
LIG_LIR_Gen_1 | 106 | 117 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 506 | 511 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 534 | 539 | PF02991 | 0.342 |
LIG_NRBOX | 289 | 295 | PF00104 | 0.511 |
LIG_NRBOX | 53 | 59 | PF00104 | 0.454 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 163 | 166 | PF00017 | 0.564 |
LIG_SH3_2 | 545 | 550 | PF14604 | 0.591 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.561 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.314 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.436 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.635 |
LIG_SH3_3 | 542 | 548 | PF00018 | 0.715 |
LIG_SUMO_SIM_par_1 | 208 | 215 | PF11976 | 0.402 |
LIG_WW_3 | 79 | 83 | PF00397 | 0.755 |
MOD_CDC14_SPxK_1 | 547 | 550 | PF00782 | 0.599 |
MOD_CDK_SPxK_1 | 544 | 550 | PF00069 | 0.585 |
MOD_CDK_SPxxK_3 | 410 | 417 | PF00069 | 0.514 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.665 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.674 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.609 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.646 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.496 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.481 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.471 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.602 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.502 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.737 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.541 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.506 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.536 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.507 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.683 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.666 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.787 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.727 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.570 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.431 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.691 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.489 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.457 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.581 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.368 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.689 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.662 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.598 |
MOD_N-GLC_2 | 236 | 238 | PF02516 | 0.487 |
MOD_N-GLC_2 | 525 | 527 | PF02516 | 0.465 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.556 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.742 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.362 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.379 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.355 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.507 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.572 |
MOD_NEK2_2 | 104 | 109 | PF00069 | 0.581 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.476 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.501 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.546 |
MOD_PK_1 | 477 | 483 | PF00069 | 0.349 |
MOD_PKA_1 | 359 | 365 | PF00069 | 0.454 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.568 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.470 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.502 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.647 |
MOD_PKB_1 | 357 | 365 | PF00069 | 0.457 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.515 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.665 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.449 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.349 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.394 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.410 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.549 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.599 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.573 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.568 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.582 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.419 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.643 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.672 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.375 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.594 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.376 |
MOD_SUMO_rev_2 | 295 | 304 | PF00179 | 0.416 |
TRG_DiLeu_BaEn_1 | 426 | 431 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 361 | 366 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.354 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 281 | 285 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 537 | 541 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 67 | 72 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEI5 | Leptomonas seymouri | 30% | 93% |
A0A3S7WSG2 | Leishmania donovani | 85% | 100% |
A4H766 | Leishmania braziliensis | 67% | 100% |
A4HVK5 | Leishmania infantum | 84% | 100% |
Q4QG77 | Leishmania major | 83% | 100% |