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: A4HHG8
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 | 321 | 325 | PF00656 | 0.434 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.441 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.438 |
CLV_PCSK_PC7_1 | 243 | 249 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.336 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.671 |
DEG_SPOP_SBC_1 | 185 | 189 | PF00917 | 0.676 |
DOC_MAPK_gen_1 | 251 | 261 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 28 | 35 | PF00069 | 0.669 |
DOC_MAPK_gen_1 | 432 | 440 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 28 | 35 | PF00069 | 0.669 |
DOC_MAPK_MEF2A_6 | 287 | 294 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 386 | 394 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 434 | 442 | PF00069 | 0.234 |
DOC_MAPK_MEF2A_6 | 478 | 487 | PF00069 | 0.615 |
DOC_MAPK_NFAT4_5 | 287 | 295 | PF00069 | 0.546 |
DOC_PP1_RVXF_1 | 217 | 223 | PF00149 | 0.620 |
DOC_PP1_RVXF_1 | 285 | 292 | PF00149 | 0.546 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.626 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.690 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.850 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 10 | 15 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 160 | 170 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 257 | 262 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 512 | 519 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 526 | 532 | PF00244 | 0.652 |
LIG_APCC_ABBA_1 | 392 | 397 | PF00400 | 0.303 |
LIG_BRCT_BRCA1_1 | 368 | 372 | PF00533 | 0.405 |
LIG_CaM_IQ_9 | 559 | 575 | PF13499 | 0.530 |
LIG_Clathr_ClatBox_1 | 378 | 382 | PF01394 | 0.405 |
LIG_eIF4E_1 | 306 | 312 | PF01652 | 0.546 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.661 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.666 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.648 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.524 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.247 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.620 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.665 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.675 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.669 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.446 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.749 |
LIG_GBD_Chelix_1 | 373 | 381 | PF00786 | 0.405 |
LIG_HCF-1_HBM_1 | 336 | 339 | PF13415 | 0.434 |
LIG_LIR_Apic_2 | 279 | 283 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.698 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 369 | 378 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 450 | 458 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 213 | 217 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 369 | 373 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.362 |
LIG_Pex14_1 | 465 | 469 | PF04695 | 0.604 |
LIG_Pex14_2 | 372 | 376 | PF04695 | 0.405 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.501 |
LIG_PTB_Apo_2 | 398 | 405 | PF02174 | 0.415 |
LIG_PTB_Phospho_1 | 398 | 404 | PF10480 | 0.415 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.518 |
LIG_SH3_1 | 332 | 338 | PF00018 | 0.546 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.640 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.635 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.434 |
LIG_Sin3_3 | 521 | 528 | PF02671 | 0.577 |
LIG_SUMO_SIM_par_1 | 153 | 158 | PF11976 | 0.652 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.685 |
LIG_SUMO_SIM_par_1 | 376 | 385 | PF11976 | 0.405 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.664 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.730 |
LIG_UBA3_1 | 507 | 513 | PF00899 | 0.571 |
MOD_CDK_SPxxK_3 | 129 | 136 | PF00069 | 0.649 |
MOD_CDK_SPxxK_3 | 471 | 478 | PF00069 | 0.434 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.681 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.706 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.662 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.683 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.578 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.651 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.656 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.434 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.682 |
MOD_Cter_Amidation | 241 | 244 | PF01082 | 0.330 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.525 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.429 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.439 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.541 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.418 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.452 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.444 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.354 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.417 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.448 |
MOD_GlcNHglycan | 9 | 13 | PF01048 | 0.488 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.683 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.661 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.735 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.692 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.689 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.440 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.359 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.494 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.730 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.647 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.442 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.668 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.712 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.636 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.546 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.593 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.544 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.559 |
MOD_NEK2_2 | 447 | 452 | PF00069 | 0.525 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.759 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.643 |
MOD_PKA_1 | 512 | 518 | PF00069 | 0.568 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.668 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.668 |
MOD_PKB_1 | 255 | 263 | PF00069 | 0.556 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.641 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.631 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.247 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.546 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.523 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.657 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.660 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.662 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.663 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.295 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.656 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.342 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.492 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.665 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.744 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.850 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.630 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.586 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.514 |
MOD_SUMO_rev_2 | 92 | 102 | PF00179 | 0.722 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 359 | 364 | PF01217 | 0.563 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.641 |
TRG_NES_CRM1_1 | 522 | 537 | PF08389 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEG1 | Leishmania donovani | 75% | 100% |
A4I4L7 | Leishmania infantum | 75% | 100% |
E9AE15 | Leishmania major | 75% | 100% |
E9ALR8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 82% |
E9AU43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |