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: A0A3S7WQM8
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 | 81 | 85 | PF00656 | 0.742 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 564 | 568 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.467 |
DEG_APCC_DBOX_1 | 406 | 414 | PF00400 | 0.493 |
DEG_SCF_FBW7_1 | 421 | 428 | PF00400 | 0.510 |
DEG_SPOP_SBC_1 | 307 | 311 | PF00917 | 0.616 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.690 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.767 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 564 | 574 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 167 | 176 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 182 | 191 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 23 | 31 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 404 | 412 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 490 | 497 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 564 | 572 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 503 | 510 | PF00149 | 0.429 |
DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.791 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.473 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 167 | 175 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 202 | 212 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 393 | 403 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 407 | 411 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 505 | 510 | PF00244 | 0.419 |
LIG_Actin_WH2_2 | 136 | 153 | PF00022 | 0.562 |
LIG_Actin_WH2_2 | 178 | 194 | PF00022 | 0.580 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 354 | 358 | PF00928 | 0.595 |
LIG_deltaCOP1_diTrp_1 | 517 | 521 | PF00928 | 0.447 |
LIG_EVH1_1 | 114 | 118 | PF00568 | 0.717 |
LIG_EVH1_2 | 118 | 122 | PF00568 | 0.716 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.487 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.671 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.485 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.659 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.498 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.437 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.416 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.716 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.572 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.647 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.660 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.520 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.522 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.715 |
LIG_GBD_Chelix_1 | 27 | 35 | PF00786 | 0.488 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 352 | 362 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 578 | 588 | PF02991 | 0.477 |
LIG_LIR_LC3C_4 | 24 | 29 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.498 |
LIG_PCNA_yPIPBox_3 | 257 | 266 | PF02747 | 0.426 |
LIG_Pex14_1 | 518 | 522 | PF04695 | 0.451 |
LIG_Pex14_2 | 34 | 38 | PF04695 | 0.514 |
LIG_Pex14_2 | 509 | 513 | PF04695 | 0.433 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.493 |
LIG_SH3_2 | 115 | 120 | PF14604 | 0.723 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.767 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.452 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.552 |
LIG_SH3_CIN85_PxpxPR_1 | 115 | 120 | PF14604 | 0.801 |
LIG_SUMO_SIM_par_1 | 27 | 32 | PF11976 | 0.507 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.606 |
LIG_TYR_ITIM | 403 | 408 | PF00017 | 0.575 |
LIG_WW_3 | 110 | 114 | PF00397 | 0.704 |
LIG_WW_3 | 117 | 121 | PF00397 | 0.633 |
MOD_CDC14_SPxK_1 | 331 | 334 | PF00782 | 0.798 |
MOD_CDK_SPxK_1 | 328 | 334 | PF00069 | 0.771 |
MOD_CDK_SPxxK_3 | 412 | 419 | PF00069 | 0.664 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.763 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.514 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.696 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.687 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.655 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.559 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.665 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.535 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.514 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.681 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.750 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.657 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.524 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.671 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.515 |
MOD_CMANNOS | 518 | 521 | PF00535 | 0.444 |
MOD_DYRK1A_RPxSP_1 | 334 | 338 | PF00069 | 0.691 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.661 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.465 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.712 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.508 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.456 |
MOD_GlcNHglycan | 368 | 373 | PF01048 | 0.460 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.728 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.702 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.672 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.514 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.844 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.493 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.524 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.734 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.567 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.598 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.491 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.504 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.660 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.588 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.698 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.439 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.603 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.782 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.779 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.695 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.637 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.445 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.754 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.462 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.756 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.482 |
MOD_PK_1 | 149 | 155 | PF00069 | 0.595 |
MOD_PK_1 | 503 | 509 | PF00069 | 0.432 |
MOD_PK_1 | 547 | 553 | PF00069 | 0.530 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.462 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.515 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.618 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.498 |
MOD_PKB_1 | 149 | 157 | PF00069 | 0.653 |
MOD_PKB_1 | 202 | 210 | PF00069 | 0.706 |
MOD_PKB_1 | 545 | 553 | PF00069 | 0.549 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.684 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.652 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.684 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.456 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.418 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.452 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.667 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.664 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.762 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.553 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.491 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.624 |
TRG_DiLeu_BaLyEn_6 | 325 | 330 | PF01217 | 0.626 |
TRG_DiLeu_BaLyEn_6 | 416 | 421 | PF01217 | 0.573 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 553 | 555 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 563 | 566 | PF00400 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 321 | 326 | PF00026 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 553 | 557 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5F1 | Leptomonas seymouri | 36% | 100% |
A4H5N2 | Leishmania braziliensis | 68% | 97% |
A4HTX6 | Leishmania infantum | 99% | 99% |
E9AMQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QHW9 | Leishmania major | 89% | 100% |