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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B0R4
Term | Name | Level | Count |
---|---|---|---|
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0043087 | regulation of GTPase activity | 5 | 1 |
GO:0043547 | positive regulation of GTPase activity | 6 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0051336 | regulation of hydrolase activity | 4 | 1 |
GO:0051345 | positive regulation of hydrolase activity | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0090630 | activation of GTPase activity | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0003924 | GTPase activity | 7 | 4 |
GO:0003925 | G protein activity | 2 | 4 |
GO:0005096 | GTPase activator activity | 4 | 1 |
GO:0008047 | enzyme activator activity | 3 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 4 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 4 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 4 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0030695 | GTPase regulator activity | 4 | 1 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 4 |
GO:0140677 | molecular function activator activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.376 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.376 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 600 | 602 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.360 |
DEG_APCC_DBOX_1 | 157 | 165 | PF00400 | 0.616 |
DEG_MDM2_SWIB_1 | 502 | 510 | PF02201 | 0.300 |
DEG_SCF_FBW7_1 | 47 | 54 | PF00400 | 0.574 |
DEG_SCF_TRCP1_1 | 149 | 154 | PF00400 | 0.536 |
DOC_AGCK_PIF_1 | 499 | 504 | PF00069 | 0.360 |
DOC_CKS1_1 | 43 | 48 | PF01111 | 0.618 |
DOC_CYCLIN_RxL_1 | 371 | 380 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 15 | 23 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 70 | 78 | PF00069 | 0.414 |
DOC_MAPK_HePTP_8 | 487 | 499 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 490 | 499 | PF00069 | 0.328 |
DOC_PP1_RVXF_1 | 372 | 378 | PF00149 | 0.360 |
DOC_PP1_RVXF_1 | 85 | 92 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.663 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.588 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.300 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.523 |
DOC_USP7_MATH_2 | 572 | 578 | PF00917 | 0.438 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.360 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 273 | 279 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 533 | 538 | PF00244 | 0.376 |
LIG_APCC_ABBA_1 | 495 | 500 | PF00400 | 0.328 |
LIG_BIR_III_2 | 239 | 243 | PF00653 | 0.697 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.551 |
LIG_BRCT_BRCA1_1 | 585 | 589 | PF00533 | 0.405 |
LIG_deltaCOP1_diTrp_1 | 101 | 110 | PF00928 | 0.387 |
LIG_eIF4E_1 | 541 | 547 | PF01652 | 0.300 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.493 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.699 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.623 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.360 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.300 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.243 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.262 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.300 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.427 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.376 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 140 | 148 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 422 | 433 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 559 | 568 | PF02991 | 0.394 |
LIG_LIR_LC3C_4 | 394 | 397 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 559 | 564 | PF02991 | 0.424 |
LIG_Pex14_1 | 449 | 453 | PF04695 | 0.360 |
LIG_Pex14_2 | 425 | 429 | PF04695 | 0.328 |
LIG_Pex14_2 | 502 | 506 | PF04695 | 0.300 |
LIG_SH2_CRK | 488 | 492 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 561 | 564 | PF00017 | 0.393 |
LIG_SH2_SRC | 131 | 134 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.236 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.625 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.609 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.611 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.713 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.503 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.336 |
LIG_SUMO_SIM_anti_2 | 559 | 566 | PF11976 | 0.405 |
LIG_SxIP_EBH_1 | 49 | 58 | PF03271 | 0.454 |
LIG_TRAF2_1 | 529 | 532 | PF00917 | 0.336 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.487 |
LIG_WW_1 | 485 | 488 | PF00397 | 0.360 |
LIG_WW_2 | 297 | 300 | PF00397 | 0.611 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.652 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.662 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.685 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.721 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.665 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.662 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.328 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.300 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.336 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.532 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.546 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.683 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.592 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.685 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.509 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.701 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.714 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.300 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.371 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.689 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.572 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.391 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.378 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.558 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.631 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.479 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.748 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.692 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.590 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.678 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.702 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.621 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.324 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.529 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.360 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.371 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.646 |
MOD_N-GLC_1 | 460 | 465 | PF02516 | 0.360 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.381 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.528 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.571 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.636 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.713 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.360 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.376 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.300 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.545 |
MOD_NEK2_2 | 595 | 600 | PF00069 | 0.402 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.484 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.716 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.376 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.300 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.328 |
MOD_PK_1 | 533 | 539 | PF00069 | 0.376 |
MOD_PKA_1 | 533 | 539 | PF00069 | 0.376 |
MOD_PKA_1 | 600 | 606 | PF00069 | 0.463 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.583 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.300 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.376 |
MOD_PKA_2 | 600 | 606 | PF00069 | 0.511 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.473 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.438 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.411 |
MOD_Plk_2-3 | 574 | 580 | PF00069 | 0.454 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.415 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.483 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.541 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.311 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.189 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.688 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.534 |
TRG_DiLeu_BaEn_2 | 100 | 106 | PF01217 | 0.375 |
TRG_DiLeu_BaEn_2 | 372 | 378 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 519 | 524 | PF01217 | 0.360 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.402 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 533 | 535 | PF00400 | 0.376 |
TRG_NES_CRM1_1 | 426 | 438 | PF08389 | 0.289 |
TRG_NES_CRM1_1 | 580 | 592 | PF08389 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 513 | 517 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 87 | 92 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3K2 | Leptomonas seymouri | 55% | 82% |
A0A3Q8IE73 | Leishmania donovani | 91% | 100% |
A4HI87 | Leishmania braziliensis | 76% | 100% |
A4I5G6 | Leishmania infantum | 91% | 100% |
Q4Q7G9 | Leishmania major | 90% | 100% |
V5BU55 | Trypanosoma cruzi | 41% | 100% |