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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
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 |
Related structures:
AlphaFold database: A4HQC7
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 | 2 |
GO:0140677 | molecular function activator activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.721 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.373 |
CLV_Separin_Metazoa | 230 | 234 | PF03568 | 0.169 |
CLV_Separin_Metazoa | 399 | 403 | PF03568 | 0.393 |
DEG_APCC_DBOX_1 | 361 | 369 | PF00400 | 0.413 |
DOC_CYCLIN_RxL_1 | 369 | 382 | PF00134 | 0.169 |
DOC_MAPK_gen_1 | 127 | 137 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 369 | 378 | PF00069 | 0.203 |
DOC_MAPK_MEF2A_6 | 358 | 367 | PF00069 | 0.251 |
DOC_MAPK_MEF2A_6 | 402 | 409 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 166 | 173 | PF00149 | 0.280 |
DOC_PP1_RVXF_1 | 404 | 410 | PF00149 | 0.451 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.475 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.672 |
DOC_USP7_UBL2_3 | 406 | 410 | PF12436 | 0.408 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 306 | 310 | PF00244 | 0.169 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.473 |
LIG_Actin_WH2_2 | 3 | 21 | PF00022 | 0.447 |
LIG_AP2alpha_1 | 107 | 111 | PF02296 | 0.382 |
LIG_APCC_ABBA_1 | 9 | 14 | PF00400 | 0.683 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.255 |
LIG_Clathr_ClatBox_1 | 367 | 371 | PF01394 | 0.368 |
LIG_CtBP_PxDLS_1 | 85 | 89 | PF00389 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 266 | 273 | PF00928 | 0.416 |
LIG_eIF4E_1 | 339 | 345 | PF01652 | 0.393 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.358 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.335 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.725 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.434 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.469 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.329 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.357 |
LIG_IRF3_LxIS_1 | 401 | 408 | PF10401 | 0.226 |
LIG_LIR_Gen_1 | 104 | 115 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 188 | 197 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 268 | 277 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 346 | 353 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.316 |
LIG_PCNA_PIPBox_1 | 309 | 318 | PF02747 | 0.413 |
LIG_Pex14_1 | 357 | 361 | PF04695 | 0.293 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.362 |
LIG_Pex14_2 | 287 | 291 | PF04695 | 0.386 |
LIG_Pex14_2 | 332 | 336 | PF04695 | 0.301 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.269 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.275 |
LIG_SH2_GRB2like | 239 | 242 | PF00017 | 0.291 |
LIG_SH2_GRB2like | 339 | 342 | PF00017 | 0.393 |
LIG_SH2_SRC | 325 | 328 | PF00017 | 0.169 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.257 |
LIG_SH2_STAT3 | 421 | 424 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.251 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.353 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.644 |
LIG_SUMO_SIM_par_1 | 374 | 383 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 384 | 390 | PF11976 | 0.385 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.370 |
LIG_UBA3_1 | 367 | 372 | PF00899 | 0.250 |
LIG_UBA3_1 | 384 | 389 | PF00899 | 0.430 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.366 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.235 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.666 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.551 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.445 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.433 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.423 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.364 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.677 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.284 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.529 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.295 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.669 |
MOD_GlcNHglycan | 87 | 91 | PF01048 | 0.632 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.664 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.511 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.700 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.664 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.644 |
MOD_N-GLC_2 | 56 | 58 | PF02516 | 0.457 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.315 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.319 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.337 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.169 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.439 |
MOD_NEK2_2 | 331 | 336 | PF00069 | 0.310 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.364 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.666 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.352 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.313 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.570 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.604 |
MOD_Plk_2-3 | 48 | 54 | PF00069 | 0.541 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.236 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.307 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.315 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.730 |
MOD_SUMO_for_1 | 368 | 371 | PF00179 | 0.316 |
MOD_SUMO_rev_2 | 194 | 202 | PF00179 | 0.284 |
MOD_SUMO_rev_2 | 390 | 397 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.310 |
TRG_DiLeu_BaEn_1 | 381 | 386 | PF01217 | 0.345 |
TRG_DiLeu_LyEn_5 | 371 | 376 | PF01217 | 0.310 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.169 |
TRG_NES_CRM1_1 | 250 | 265 | PF08389 | 0.335 |
TRG_NLS_MonoExtN_4 | 127 | 132 | PF00514 | 0.319 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3T4 | Leptomonas seymouri | 53% | 99% |
A0A0N1PDX9 | Leptomonas seymouri | 41% | 77% |
A0A0S4II34 | Bodo saltans | 35% | 100% |
A0A0S4ITU5 | Bodo saltans | 27% | 100% |
A0A1X0NLM2 | Trypanosomatidae | 43% | 100% |
A0A1X0NLQ9 | Trypanosomatidae | 42% | 100% |
A0A3Q8IEG1 | Leishmania donovani | 27% | 81% |
A0A3S7X3S6 | Leishmania donovani | 26% | 100% |
A0A3S7XBZ8 | Leishmania donovani | 72% | 100% |
A0A3S7XC15 | Leishmania donovani | 40% | 86% |
A0A422NJ84 | Trypanosoma rangeli | 41% | 100% |
A0A422NJE8 | Trypanosoma rangeli | 43% | 100% |
A4HIL7 | Leishmania braziliensis | 25% | 100% |
A4HQC6 | Leishmania braziliensis | 41% | 87% |
A4I4L7 | Leishmania infantum | 27% | 81% |
A4I5W2 | Leishmania infantum | 25% | 100% |
A4IE19 | Leishmania infantum | 40% | 86% |
A4IE20 | Leishmania infantum | 72% | 100% |
D0A3X9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AE15 | Leishmania major | 26% | 81% |
E9AU42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 76% |
E9AU43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9B157 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
P58802 | Mus musculus | 32% | 85% |
Q09844 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 90% |
Q4Q0F2 | Leishmania major | 71% | 99% |
Q4Q0F3 | Leishmania major | 37% | 100% |
Q6GL87 | Xenopus tropicalis | 29% | 100% |
Q9BXI6 | Homo sapiens | 32% | 84% |
Q9VGL8 | Drosophila melanogaster | 30% | 100% |
V5BT66 | Trypanosoma cruzi | 38% | 100% |