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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000331 | contractile vacuole | 6 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AU42
Term | Name | Level | Count |
---|---|---|---|
GO:0043085 | positive regulation of catalytic activity | 4 | 2 |
GO:0043087 | regulation of GTPase activity | 5 | 2 |
GO:0043547 | positive regulation of GTPase activity | 6 | 2 |
GO:0044093 | positive regulation of molecular function | 3 | 2 |
GO:0050790 | regulation of catalytic activity | 3 | 2 |
GO:0051336 | regulation of hydrolase activity | 4 | 2 |
GO:0051345 | positive regulation of hydrolase activity | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065009 | regulation of molecular function | 2 | 2 |
GO:0090630 | activation of GTPase activity | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 2 |
GO:0008047 | enzyme activator activity | 3 | 2 |
GO:0030234 | enzyme regulator activity | 2 | 2 |
GO:0030695 | GTPase regulator activity | 4 | 2 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 2 |
GO:0098772 | molecular function regulator activity | 1 | 4 |
GO:0140677 | molecular function activator activity | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0003924 | GTPase activity | 7 | 2 |
GO:0003925 | G protein activity | 2 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 523 | 527 | PF00656 | 0.406 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.410 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.236 |
CLV_PCSK_PC1ET2_1 | 446 | 448 | PF00082 | 0.226 |
CLV_PCSK_PC7_1 | 259 | 265 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.345 |
CLV_Separin_Metazoa | 529 | 533 | PF03568 | 0.391 |
DEG_MDM2_SWIB_1 | 458 | 466 | PF02201 | 0.315 |
DEG_MDM2_SWIB_1 | 484 | 491 | PF02201 | 0.304 |
DOC_CKS1_1 | 204 | 209 | PF01111 | 0.608 |
DOC_CYCLIN_RxL_1 | 470 | 481 | PF00134 | 0.232 |
DOC_MAPK_gen_1 | 443 | 453 | PF00069 | 0.286 |
DOC_MAPK_gen_1 | 532 | 539 | PF00069 | 0.374 |
DOC_PP1_RVXF_1 | 262 | 269 | PF00149 | 0.332 |
DOC_PP1_RVXF_1 | 297 | 304 | PF00149 | 0.271 |
DOC_PP1_RVXF_1 | 487 | 493 | PF00149 | 0.259 |
DOC_PP1_RVXF_1 | 534 | 540 | PF00149 | 0.375 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.296 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.230 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.682 |
DOC_USP7_UBL2_3 | 281 | 285 | PF12436 | 0.368 |
DOC_USP7_UBL2_3 | 329 | 333 | PF12436 | 0.315 |
DOC_USP7_UBL2_3 | 60 | 64 | PF12436 | 0.490 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.715 |
LIG_14-3-3_CanoR_1 | 179 | 187 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 49 | 53 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 171 | 186 | PF00022 | 0.477 |
LIG_BRCT_BRCA1_1 | 459 | 463 | PF00533 | 0.260 |
LIG_deltaCOP1_diTrp_1 | 265 | 275 | PF00928 | 0.372 |
LIG_deltaCOP1_diTrp_1 | 486 | 492 | PF00928 | 0.259 |
LIG_eIF4E_1 | 413 | 419 | PF01652 | 0.312 |
LIG_eIF4E_1 | 83 | 89 | PF01652 | 0.454 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.517 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.582 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.500 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.307 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.327 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.252 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.316 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.646 |
LIG_GBD_Chelix_1 | 387 | 395 | PF00786 | 0.260 |
LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 265 | 273 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 309 | 317 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 460 | 471 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 526 | 534 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 549 | 558 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 98 | 106 | PF02991 | 0.518 |
LIG_LIR_LC3C_4 | 114 | 119 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.519 |
LIG_OCRL_FandH_1 | 400 | 412 | PF00620 | 0.259 |
LIG_PALB2_WD40_1 | 458 | 466 | PF16756 | 0.232 |
LIG_PAM2_1 | 453 | 465 | PF00658 | 0.279 |
LIG_Pex14_1 | 480 | 484 | PF04695 | 0.328 |
LIG_Pex14_1 | 488 | 492 | PF04695 | 0.318 |
LIG_Pex14_2 | 419 | 423 | PF04695 | 0.315 |
LIG_Pex14_2 | 458 | 462 | PF04695 | 0.285 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.280 |
LIG_Pex14_2 | 484 | 488 | PF04695 | 0.321 |
LIG_PTB_Apo_2 | 407 | 414 | PF02174 | 0.382 |
LIG_PTB_Phospho_1 | 407 | 413 | PF10480 | 0.382 |
LIG_REV1ctd_RIR_1 | 428 | 439 | PF16727 | 0.186 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.505 |
LIG_SH2_PTP2 | 322 | 325 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.476 |
LIG_SH2_STAT3 | 83 | 86 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.301 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.602 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.266 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.498 |
LIG_SUMO_SIM_anti_2 | 113 | 120 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 494 | 500 | PF11976 | 0.315 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.551 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.567 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.254 |
LIG_UBA3_1 | 440 | 446 | PF00899 | 0.311 |
LIG_UBA3_1 | 515 | 519 | PF00899 | 0.374 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.315 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.739 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.761 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.651 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.534 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.534 |
MOD_Cter_Amidation | 47 | 50 | PF01082 | 0.484 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.549 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.672 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.500 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.774 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.624 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.704 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.258 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.558 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.295 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.592 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.625 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.428 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.631 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.297 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.308 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.269 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.297 |
MOD_NEK2_2 | 462 | 467 | PF00069 | 0.301 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.718 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.636 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.232 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.232 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.787 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.562 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.628 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.292 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.500 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.589 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.531 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.259 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.320 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.359 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.625 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.484 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.485 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.240 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.263 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.301 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.349 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.291 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.520 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.557 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.597 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.667 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.714 |
MOD_SUMO_for_1 | 499 | 502 | PF00179 | 0.281 |
MOD_SUMO_rev_2 | 243 | 253 | PF00179 | 0.518 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.281 |
TRG_DiLeu_BaEn_1 | 553 | 558 | PF01217 | 0.336 |
TRG_DiLeu_BaEn_2 | 3 | 9 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_4 | 502 | 508 | PF01217 | 0.271 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 421 | 426 | PF01217 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDX9 | Leptomonas seymouri | 64% | 100% |
A0A0S4II34 | Bodo saltans | 54% | 100% |
A0A3Q8IEG1 | Leishmania donovani | 28% | 100% |
A0A3S7XBZ8 | Leishmania donovani | 35% | 100% |
A0A3S7XC15 | Leishmania donovani | 89% | 100% |
A4HQC6 | Leishmania braziliensis | 79% | 100% |
A4HQC7 | Leishmania braziliensis | 40% | 100% |
A4I4L7 | Leishmania infantum | 28% | 100% |
A4IE19 | Leishmania infantum | 90% | 100% |
A4IE20 | Leishmania infantum | 35% | 100% |
E9AU43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
M0R7T9 | Rattus norvegicus | 25% | 81% |
O60347 | Homo sapiens | 26% | 72% |
Q4Q0F2 | Leishmania major | 42% | 100% |
Q4Q0F3 | Leishmania major | 88% | 100% |
Q6A039 | Mus musculus | 25% | 81% |
V5BT66 | Trypanosoma cruzi | 55% | 100% |