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: A4H766
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 | 251 | 255 | PF00656 | 0.668 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.559 |
CLV_PCSK_PC7_1 | 61 | 67 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.592 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.517 |
DEG_SCF_FBW7_1 | 411 | 417 | PF00400 | 0.468 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.602 |
DEG_SPOP_SBC_1 | 317 | 321 | PF00917 | 0.514 |
DEG_SPOP_SBC_1 | 397 | 401 | PF00917 | 0.455 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.510 |
DOC_ANK_TNKS_1 | 130 | 137 | PF00023 | 0.572 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.424 |
DOC_CKS1_1 | 411 | 416 | PF01111 | 0.476 |
DOC_CYCLIN_RxL_1 | 61 | 72 | PF00134 | 0.488 |
DOC_MAPK_gen_1 | 61 | 70 | PF00069 | 0.513 |
DOC_MAPK_HePTP_8 | 520 | 532 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 523 | 532 | PF00069 | 0.408 |
DOC_MAPK_RevD_3 | 51 | 66 | PF00069 | 0.452 |
DOC_PP4_FxxP_1 | 439 | 442 | PF00568 | 0.415 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.827 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 131 | 135 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 157 | 166 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 362 | 366 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 499 | 509 | PF00244 | 0.534 |
LIG_Actin_WH2_2 | 267 | 285 | PF00022 | 0.490 |
LIG_Actin_WH2_2 | 484 | 501 | PF00022 | 0.452 |
LIG_ActinCP_TwfCPI_2 | 439 | 448 | PF01115 | 0.465 |
LIG_BIR_III_4 | 376 | 380 | PF00653 | 0.432 |
LIG_Clathr_ClatBox_1 | 488 | 492 | PF01394 | 0.356 |
LIG_CSL_BTD_1 | 148 | 151 | PF09270 | 0.605 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.682 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.438 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.535 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.439 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.466 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.414 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.643 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.474 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.545 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.399 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.513 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.474 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.469 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.396 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.442 |
LIG_NRBOX | 52 | 58 | PF00104 | 0.510 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.327 |
LIG_SH2_STAT3 | 165 | 168 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.457 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.563 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.454 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.635 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.453 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.711 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.478 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.322 |
LIG_TRAF2_1 | 87 | 90 | PF00917 | 0.551 |
LIG_TYR_ITIM | 488 | 493 | PF00017 | 0.349 |
LIG_UBA3_1 | 536 | 541 | PF00899 | 0.289 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.555 |
MOD_CDK_SPxxK_3 | 414 | 421 | PF00069 | 0.507 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.513 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.585 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.735 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.744 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.422 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.659 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.362 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.455 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.524 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.490 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.475 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.550 |
MOD_CMANNOS | 540 | 543 | PF00535 | 0.306 |
MOD_DYRK1A_RPxSP_1 | 545 | 549 | PF00069 | 0.425 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.768 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.705 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.612 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.613 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.583 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.621 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.744 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.372 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.567 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.318 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.555 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.666 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.613 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.513 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.693 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.717 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.478 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.750 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.627 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.449 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.587 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.509 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.495 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.385 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.635 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.521 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.681 |
MOD_N-GLC_2 | 529 | 531 | PF02516 | 0.456 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.617 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.343 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.397 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.407 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.608 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.538 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.442 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.712 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.395 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.483 |
MOD_PK_1 | 481 | 487 | PF00069 | 0.359 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.571 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.457 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.512 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.514 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.606 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.381 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.695 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.507 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.387 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.359 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.322 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.450 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.414 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.634 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.601 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.413 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.546 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.433 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.453 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.655 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.446 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.387 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.588 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.607 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.399 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.679 |
MOD_SUMO_rev_2 | 87 | 93 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_2 | 429 | 435 | PF01217 | 0.334 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.494 |
TRG_NLS_MonoExtN_4 | 61 | 68 | PF00514 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 66 | 71 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEI5 | Leptomonas seymouri | 31% | 94% |
A0A3S7WSG2 | Leishmania donovani | 69% | 100% |
A4HVK5 | Leishmania infantum | 69% | 100% |
E9APA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QG77 | Leishmania major | 68% | 99% |