Phosphatase, Histidine phosphatase superfamily
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HT40
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.329 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 602 | 604 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.648 |
CLV_Separin_Metazoa | 402 | 406 | PF03568 | 0.494 |
DEG_APCC_DBOX_1 | 20 | 28 | PF00400 | 0.484 |
DEG_SPOP_SBC_1 | 624 | 628 | PF00917 | 0.686 |
DOC_CDC14_PxL_1 | 422 | 430 | PF14671 | 0.354 |
DOC_CYCLIN_RxL_1 | 433 | 441 | PF00134 | 0.442 |
DOC_CYCLIN_RxL_1 | 505 | 513 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 525 | 533 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 9 | 19 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 11 | 19 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 228 | 236 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 495 | 503 | PF00069 | 0.425 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 432 | 435 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.433 |
DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.627 |
DOC_USP7_UBL2_3 | 124 | 128 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 71 | 75 | PF12436 | 0.764 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 139 | 149 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 552 | 559 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 594 | 600 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 603 | 607 | PF00244 | 0.420 |
LIG_14-3-3_CterR_2 | 631 | 635 | PF00244 | 0.599 |
LIG_APCC_ABBA_1 | 385 | 390 | PF00400 | 0.435 |
LIG_BIR_III_2 | 241 | 245 | PF00653 | 0.409 |
LIG_deltaCOP1_diTrp_1 | 568 | 575 | PF00928 | 0.386 |
LIG_eIF4E_1 | 388 | 394 | PF01652 | 0.438 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.423 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.392 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.437 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.411 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.421 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.348 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.469 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.400 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.734 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.370 |
LIG_GBD_Chelix_1 | 536 | 544 | PF00786 | 0.351 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 318 | 329 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 424 | 428 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.547 |
LIG_LYPXL_yS_3 | 425 | 428 | PF13949 | 0.460 |
LIG_NRBOX | 427 | 433 | PF00104 | 0.440 |
LIG_PCNA_yPIPBox_3 | 582 | 591 | PF02747 | 0.432 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.520 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.431 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.396 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.568 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.388 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.447 |
LIG_SUMO_SIM_anti_2 | 13 | 19 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.504 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.485 |
LIG_TYR_ITIM | 319 | 324 | PF00017 | 0.473 |
LIG_TYR_ITIM | 423 | 428 | PF00017 | 0.411 |
LIG_TYR_ITSM | 296 | 303 | PF00017 | 0.439 |
LIG_UBA3_1 | 379 | 386 | PF00899 | 0.289 |
LIG_UBA3_1 | 517 | 525 | PF00899 | 0.428 |
LIG_WRC_WIRS_1 | 368 | 373 | PF05994 | 0.631 |
MOD_CDK_SPK_2 | 240 | 245 | PF00069 | 0.501 |
MOD_CDK_SPK_2 | 617 | 622 | PF00069 | 0.551 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.471 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.667 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.631 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.606 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.693 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.498 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.584 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.467 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.726 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.623 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.441 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.483 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.506 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.570 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.685 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.331 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.491 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.618 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.596 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.397 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.497 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.511 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.516 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.550 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.558 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.427 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.597 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.465 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.706 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.399 |
MOD_N-GLC_1 | 607 | 612 | PF02516 | 0.605 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.662 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.522 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.433 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.347 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.657 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.349 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.400 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.702 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.397 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.697 |
MOD_NEK2_2 | 315 | 320 | PF00069 | 0.396 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.478 |
MOD_PKA_1 | 602 | 608 | PF00069 | 0.437 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.667 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.333 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.571 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.682 |
MOD_Plk_2-3 | 281 | 287 | PF00069 | 0.536 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.496 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.468 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.524 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.450 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.594 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.421 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.677 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.700 |
MOD_SUMO_rev_2 | 254 | 264 | PF00179 | 0.426 |
TRG_DiLeu_BaEn_1 | 363 | 368 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 375 | 380 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 453 | 458 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.487 |
TRG_NES_CRM1_1 | 26 | 38 | PF08389 | 0.517 |
TRG_NES_CRM1_1 | 366 | 381 | PF08389 | 0.470 |
TRG_NLS_MonoCore_2 | 600 | 605 | PF00514 | 0.387 |
TRG_NLS_MonoExtC_3 | 601 | 607 | PF00514 | 0.394 |
TRG_NLS_MonoExtN_4 | 601 | 606 | PF00514 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7J6 | Leptomonas seymouri | 61% | 99% |
A0A0S4JT20 | Bodo saltans | 28% | 100% |
A0A1X0NKC6 | Trypanosomatidae | 36% | 100% |
A0A3R7NMJ1 | Trypanosoma rangeli | 32% | 100% |
A0A3S5H5W7 | Leishmania donovani | 100% | 100% |
A4H4W6 | Leishmania braziliensis | 74% | 97% |
C9ZUU8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AL32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QIS2 | Leishmania major | 94% | 100% |
V5B8V4 | Trypanosoma cruzi | 32% | 100% |