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: A4HI87
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 | 5 |
GO:0003924 | GTPase activity | 7 | 5 |
GO:0003925 | G protein activity | 2 | 5 |
GO:0016462 | pyrophosphatase activity | 5 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 5 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 5 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 5 |
GO:0098772 | molecular function regulator activity | 1 | 5 |
GO:0005096 | GTPase activator activity | 4 | 1 |
GO:0008047 | enzyme activator activity | 3 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0030695 | GTPase regulator activity | 4 | 1 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 1 |
GO:0140677 | molecular function activator activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.700 |
CLV_C14_Caspase3-7 | 576 | 580 | PF00656 | 0.388 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.388 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.312 |
CLV_Separin_Metazoa | 423 | 427 | PF03568 | 0.532 |
DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.667 |
DEG_APCC_DBOX_1 | 418 | 426 | PF00400 | 0.532 |
DEG_APCC_DBOX_1 | 96 | 104 | PF00400 | 0.502 |
DEG_COP1_1 | 288 | 300 | PF00400 | 0.527 |
DEG_MDM2_SWIB_1 | 621 | 629 | PF02201 | 0.312 |
DEG_SCF_FBW7_1 | 155 | 162 | PF00400 | 0.622 |
DEG_SCF_FBW7_1 | 281 | 288 | PF00400 | 0.549 |
DEG_SCF_FBW7_1 | 384 | 390 | PF00400 | 0.544 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.594 |
DOC_AGCK_PIF_1 | 618 | 623 | PF00069 | 0.312 |
DOC_CKS1_1 | 151 | 156 | PF01111 | 0.648 |
DOC_CKS1_1 | 384 | 389 | PF01111 | 0.542 |
DOC_CYCLIN_RxL_1 | 490 | 499 | PF00134 | 0.312 |
DOC_MAPK_gen_1 | 94 | 103 | PF00069 | 0.531 |
DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.364 |
DOC_PP1_RVXF_1 | 491 | 497 | PF00149 | 0.312 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.668 |
DOC_PP2B_LxvP_1 | 349 | 352 | PF13499 | 0.556 |
DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.597 |
DOC_PP2B_LxvP_1 | 514 | 517 | PF13499 | 0.312 |
DOC_PP2B_LxvP_1 | 687 | 690 | PF13499 | 0.280 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.496 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.604 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.312 |
DOC_USP7_MATH_2 | 691 | 697 | PF00917 | 0.472 |
DOC_USP7_UBL2_3 | 466 | 470 | PF12436 | 0.388 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 266 | 270 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 305 | 310 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 392 | 400 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 526 | 533 | PF00244 | 0.237 |
LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 652 | 657 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 97 | 101 | PF00244 | 0.663 |
LIG_Actin_WH2_2 | 289 | 307 | PF00022 | 0.524 |
LIG_BIR_III_2 | 359 | 363 | PF00653 | 0.636 |
LIG_BRCT_BRCA1_1 | 704 | 708 | PF00533 | 0.357 |
LIG_deltaCOP1_diTrp_1 | 209 | 218 | PF00928 | 0.341 |
LIG_eIF4E_1 | 660 | 666 | PF01652 | 0.312 |
LIG_EVH1_1 | 384 | 388 | PF00568 | 0.539 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.542 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.312 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.312 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.312 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.235 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.312 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.462 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.541 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.388 |
LIG_LIR_Apic_2 | 138 | 142 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 248 | 256 | PF02991 | 0.405 |
LIG_LIR_LC3C_4 | 513 | 516 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.658 |
LIG_LYPXL_yS_3 | 12 | 15 | PF13949 | 0.502 |
LIG_MYND_1 | 327 | 331 | PF01753 | 0.531 |
LIG_MYND_1 | 59 | 63 | PF01753 | 0.541 |
LIG_Pex14_1 | 568 | 572 | PF04695 | 0.312 |
LIG_Pex14_2 | 621 | 625 | PF04695 | 0.312 |
LIG_PTB_Apo_2 | 238 | 245 | PF02174 | 0.314 |
LIG_PTB_Phospho_1 | 238 | 244 | PF10480 | 0.313 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.568 |
LIG_SH2_CRK | 607 | 611 | PF00017 | 0.312 |
LIG_SH2_GRB2like | 239 | 242 | PF00017 | 0.309 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 714 | 718 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 646 | 649 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.234 |
LIG_SH3_2 | 328 | 333 | PF14604 | 0.538 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.534 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.691 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.660 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.687 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.545 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.532 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.298 |
LIG_TYR_ITIM | 10 | 15 | PF00017 | 0.483 |
LIG_TYR_ITSM | 41 | 48 | PF00017 | 0.589 |
LIG_WRC_WIRS_1 | 103 | 108 | PF05994 | 0.513 |
LIG_WW_1 | 604 | 607 | PF00397 | 0.312 |
LIG_WW_3 | 416 | 420 | PF00397 | 0.532 |
MOD_CDK_SPxxK_3 | 150 | 157 | PF00069 | 0.681 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.567 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.589 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.588 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.566 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.635 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.640 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.702 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.231 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.628 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.630 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.542 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.312 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.549 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.711 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.593 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.537 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.425 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.516 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.636 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.696 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.556 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.637 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.728 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.552 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.656 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.702 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.312 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.372 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.565 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.275 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.538 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.693 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.619 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.541 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.618 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.351 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.426 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.297 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.615 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.523 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.529 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.748 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.684 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.665 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.636 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.635 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.312 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.312 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.387 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.339 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.618 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.599 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.316 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.538 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.698 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.388 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.549 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.312 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.348 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.572 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.526 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.552 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.575 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.771 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.312 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.231 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.388 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.312 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.616 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.523 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.709 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.642 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.470 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.388 |
MOD_PIKK_1 | 634 | 640 | PF00454 | 0.312 |
MOD_PK_1 | 652 | 658 | PF00069 | 0.388 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.560 |
MOD_PKA_1 | 652 | 658 | PF00069 | 0.388 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.567 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.693 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.312 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.667 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.388 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.528 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.670 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.366 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.324 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.599 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.662 |
MOD_Plk_1 | 714 | 720 | PF00069 | 0.396 |
MOD_Plk_2-3 | 693 | 699 | PF00069 | 0.407 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.487 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.516 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.344 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.541 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.553 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.312 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.312 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.525 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.623 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.563 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.531 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.685 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.538 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.590 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.595 |
TRG_DiLeu_BaEn_2 | 208 | 214 | PF01217 | 0.328 |
TRG_DiLeu_BaEn_2 | 491 | 497 | PF01217 | 0.312 |
TRG_DiLeu_BaLyEn_6 | 325 | 330 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 638 | 643 | PF01217 | 0.312 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.388 |
TRG_NES_CRM1_1 | 699 | 711 | PF08389 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 195 | 200 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 632 | 636 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 698 | 702 | PF00026 | 0.349 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3K2 | Leptomonas seymouri | 49% | 98% |
A0A3Q8IE73 | Leishmania donovani | 78% | 100% |
A4I5G6 | Leishmania infantum | 77% | 100% |
E9B0R4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q7G9 | Leishmania major | 75% | 98% |