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: A0A3S7WSG2
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 | 247 | 251 | PF00656 | 0.653 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.524 |
CLV_PCSK_FUR_1 | 355 | 359 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.572 |
CLV_PCSK_PC7_1 | 62 | 68 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.570 |
DEG_APCC_DBOX_1 | 108 | 116 | PF00400 | 0.500 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.574 |
DOC_CKS1_1 | 359 | 364 | PF01111 | 0.415 |
DOC_CKS1_1 | 541 | 546 | PF01111 | 0.546 |
DOC_CYCLIN_RxL_1 | 62 | 73 | PF00134 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 444 | 450 | PF00134 | 0.565 |
DOC_CYCLIN_yCln2_LP_2 | 461 | 467 | PF00134 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 541 | 547 | PF00134 | 0.551 |
DOC_MAPK_gen_1 | 62 | 71 | PF00069 | 0.539 |
DOC_MAPK_HePTP_8 | 515 | 527 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 518 | 527 | PF00069 | 0.424 |
DOC_MAPK_RevD_3 | 52 | 67 | PF00069 | 0.476 |
DOC_PP2B_LxvP_1 | 461 | 464 | PF13499 | 0.469 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 121 | 126 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 357 | 362 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 420 | 430 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 494 | 504 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 536 | 540 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 82 | 89 | PF00244 | 0.601 |
LIG_Actin_WH2_2 | 263 | 281 | PF00022 | 0.478 |
LIG_Actin_WH2_2 | 419 | 437 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 479 | 496 | PF00022 | 0.454 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.545 |
LIG_Clathr_ClatBox_1 | 483 | 487 | PF01394 | 0.375 |
LIG_CSL_BTD_1 | 144 | 147 | PF09270 | 0.641 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.575 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.435 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.434 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.411 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.452 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.454 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.501 |
LIG_GBD_Chelix_1 | 284 | 292 | PF00786 | 0.419 |
LIG_LIR_Gen_1 | 104 | 115 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 407 | 415 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.408 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.438 |
LIG_NRBOX | 53 | 59 | PF00104 | 0.513 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.483 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.536 |
LIG_SH3_2 | 544 | 549 | PF14604 | 0.585 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.602 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.530 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.451 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.740 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.723 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.604 |
LIG_SUMO_SIM_par_1 | 206 | 213 | PF11976 | 0.423 |
LIG_TYR_ITIM | 483 | 488 | PF00017 | 0.368 |
LIG_UBA3_1 | 70 | 75 | PF00899 | 0.558 |
LIG_WW_3 | 79 | 83 | PF00397 | 0.616 |
MOD_CDC14_SPxK_1 | 546 | 549 | PF00782 | 0.591 |
MOD_CDK_SPxK_1 | 543 | 549 | PF00069 | 0.578 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.593 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.464 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.607 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.639 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.592 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.462 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.482 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.601 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.569 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.504 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.569 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.633 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.575 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.545 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.512 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.709 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.619 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.515 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.721 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.502 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.630 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.512 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.472 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.508 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.629 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.519 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.432 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.395 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.574 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.595 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.578 |
MOD_N-GLC_2 | 524 | 526 | PF02516 | 0.437 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.498 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.517 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.622 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.602 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.477 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.408 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.442 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.535 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.593 |
MOD_NEK2_2 | 102 | 107 | PF00069 | 0.541 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.468 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.460 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.487 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.558 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.348 |
MOD_PK_1 | 476 | 482 | PF00069 | 0.370 |
MOD_PKA_1 | 357 | 363 | PF00069 | 0.451 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.564 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.537 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.494 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.433 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.623 |
MOD_PKB_1 | 355 | 363 | PF00069 | 0.452 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.535 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.409 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.596 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.383 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.553 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.465 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.370 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.458 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.380 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.570 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.583 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.554 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.530 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.474 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.424 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.607 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.381 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.709 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.459 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.614 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.644 |
TRG_DiLeu_BaEn_1 | 425 | 430 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 359 | 364 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.448 |
TRG_NLS_MonoExtN_4 | 62 | 69 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 279 | 283 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEI5 | Leptomonas seymouri | 29% | 93% |
A4H766 | Leishmania braziliensis | 69% | 100% |
A4HVK5 | Leishmania infantum | 99% | 100% |
E9APA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QG77 | Leishmania major | 90% | 100% |