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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9ALR8
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 | 141 | 145 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 697 | 699 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.448 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.433 |
DEG_SCF_TRCP1_1 | 308 | 314 | PF00400 | 0.643 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.657 |
DEG_SPOP_SBC_1 | 55 | 59 | PF00917 | 0.641 |
DOC_CKS1_1 | 262 | 267 | PF01111 | 0.802 |
DOC_CKS1_1 | 330 | 335 | PF01111 | 0.738 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.680 |
DOC_CYCLIN_yClb3_PxF_3 | 466 | 474 | PF00134 | 0.580 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.656 |
DOC_CYCLIN_yCln2_LP_2 | 330 | 336 | PF00134 | 0.575 |
DOC_MAPK_gen_1 | 160 | 167 | PF00069 | 0.715 |
DOC_MAPK_gen_1 | 382 | 392 | PF00069 | 0.674 |
DOC_MAPK_gen_1 | 563 | 571 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 673 | 681 | PF00069 | 0.647 |
DOC_MAPK_MEF2A_6 | 160 | 167 | PF00069 | 0.715 |
DOC_MAPK_MEF2A_6 | 418 | 425 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 517 | 525 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 609 | 618 | PF00069 | 0.636 |
DOC_MAPK_NFAT4_5 | 418 | 426 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 348 | 354 | PF00149 | 0.706 |
DOC_PP1_RVXF_1 | 416 | 423 | PF00149 | 0.636 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.659 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.730 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.629 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.818 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.650 |
DOC_USP7_MATH_2 | 265 | 271 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 378 | 382 | PF12436 | 0.715 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.848 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 245 | 249 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 388 | 393 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 643 | 650 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 657 | 663 | PF00244 | 0.512 |
LIG_Actin_WH2_2 | 403 | 420 | PF00022 | 0.620 |
LIG_Actin_WH2_2 | 688 | 706 | PF00022 | 0.520 |
LIG_APCC_ABBA_1 | 523 | 528 | PF00400 | 0.366 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.634 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.626 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.617 |
LIG_Clathr_ClatBox_1 | 509 | 513 | PF01394 | 0.530 |
LIG_deltaCOP1_diTrp_1 | 28 | 32 | PF00928 | 0.645 |
LIG_eIF4E_1 | 437 | 443 | PF01652 | 0.636 |
LIG_eIF4E_1 | 650 | 656 | PF01652 | 0.603 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.681 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.650 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.634 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.521 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.380 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.660 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.604 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.741 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.825 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.692 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.683 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.613 |
LIG_GBD_Chelix_1 | 504 | 512 | PF00786 | 0.530 |
LIG_LIR_Apic_2 | 102 | 108 | PF02991 | 0.655 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 80 | 86 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 344 | 353 | PF02991 | 0.712 |
LIG_LIR_Gen_1 | 500 | 509 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 518 | 526 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 581 | 590 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 500 | 504 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 581 | 586 | PF02991 | 0.530 |
LIG_PCNA_yPIPBox_3 | 546 | 559 | PF02747 | 0.380 |
LIG_Pex14_1 | 596 | 600 | PF04695 | 0.636 |
LIG_Pex14_2 | 503 | 507 | PF04695 | 0.369 |
LIG_Pex14_2 | 583 | 587 | PF04695 | 0.530 |
LIG_PTB_Apo_2 | 529 | 536 | PF02174 | 0.435 |
LIG_PTB_Phospho_1 | 529 | 535 | PF10480 | 0.435 |
LIG_SH2_NCK_1 | 650 | 654 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 650 | 654 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.636 |
LIG_SH3_1 | 259 | 265 | PF00018 | 0.722 |
LIG_SH3_1 | 463 | 469 | PF00018 | 0.636 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.806 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.738 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.588 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.482 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.633 |
LIG_Sin3_3 | 652 | 659 | PF02671 | 0.660 |
LIG_SUMO_SIM_par_1 | 162 | 169 | PF11976 | 0.740 |
LIG_SUMO_SIM_par_1 | 507 | 516 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 677 | 682 | PF11976 | 0.654 |
MOD_CDK_SPK_2 | 662 | 667 | PF00069 | 0.649 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.642 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.692 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.726 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.743 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.717 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.706 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.748 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.655 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.705 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.688 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.671 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.442 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.491 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.604 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.442 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.613 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.574 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.490 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.472 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.412 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.488 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.420 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.428 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.551 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.415 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.634 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.692 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.771 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.721 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.761 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.836 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.593 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.702 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.541 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.652 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.508 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.623 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.676 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.649 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.458 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.444 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.661 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.748 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.786 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.687 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.636 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.655 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.636 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.660 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.438 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.795 |
MOD_NEK2_2 | 578 | 583 | PF00069 | 0.369 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.644 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.752 |
MOD_PKA_1 | 280 | 286 | PF00069 | 0.799 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.715 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.670 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.716 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.745 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.686 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.715 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.626 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.395 |
MOD_Plk_1 | 614 | 620 | PF00069 | 0.636 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.697 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.702 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.435 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.313 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.422 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.365 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.657 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.676 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.850 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.802 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.647 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.676 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.696 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.636 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.553 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.649 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.650 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.626 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 227 | 234 | PF00179 | 0.768 |
MOD_SUMO_rev_2 | 550 | 558 | PF00179 | 0.380 |
TRG_DiLeu_BaEn_1 | 229 | 234 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_4 | 229 | 235 | PF01217 | 0.662 |
TRG_DiLeu_BaLyEn_6 | 490 | 495 | PF01217 | 0.636 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 672 | 674 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 697 | 699 | PF00400 | 0.733 |
TRG_ER_diArg_1 | 703 | 705 | PF00400 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 411 | 415 | PF00026 | 0.262 |
TRG_Pf-PMV_PEXEL_1 | 697 | 701 | PF00026 | 0.320 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEG1 | Leishmania donovani | 91% | 100% |
A4HHG8 | Leishmania braziliensis | 73% | 100% |
A4I4L7 | Leishmania infantum | 91% | 100% |
E9AE15 | Leishmania major | 89% | 100% |