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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QB89
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005525 | GTP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0019001 | guanyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.359 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.568 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.493 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.469 |
DEG_SCF_FBW7_1 | 127 | 134 | PF00400 | 0.580 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.670 |
DOC_CKS1_1 | 195 | 200 | PF01111 | 0.488 |
DOC_CKS1_1 | 232 | 237 | PF01111 | 0.415 |
DOC_CYCLIN_yClb1_LxF_4 | 206 | 212 | PF00134 | 0.440 |
DOC_MAPK_DCC_7 | 167 | 176 | PF00069 | 0.554 |
DOC_MAPK_gen_1 | 379 | 388 | PF00069 | 0.294 |
DOC_MAPK_MEF2A_6 | 167 | 176 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 70 | 77 | PF00149 | 0.519 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.683 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.611 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 167 | 171 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 179 | 187 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 267 | 273 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 72 | 77 | PF00244 | 0.580 |
LIG_Actin_WH2_2 | 188 | 205 | PF00022 | 0.488 |
LIG_BIR_III_2 | 359 | 363 | PF00653 | 0.412 |
LIG_BRCT_BRCA1_1 | 207 | 211 | PF00533 | 0.453 |
LIG_eIF4E_1 | 338 | 344 | PF01652 | 0.423 |
LIG_eIF4E_1 | 372 | 378 | PF01652 | 0.438 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.451 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.423 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.610 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.358 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.560 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.480 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.328 |
LIG_GBD_Chelix_1 | 187 | 195 | PF00786 | 0.330 |
LIG_LIR_Apic_2 | 345 | 350 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 418 | 425 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.488 |
LIG_PCNA_yPIPBox_3 | 184 | 196 | PF02747 | 0.439 |
LIG_PDZ_Class_1 | 420 | 425 | PF00595 | 0.561 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.394 |
LIG_SH2_NCK_1 | 212 | 216 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.624 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.428 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.699 |
LIG_SUMO_SIM_par_1 | 118 | 123 | PF11976 | 0.468 |
LIG_WRC_WIRS_1 | 404 | 409 | PF05994 | 0.505 |
MOD_CDC14_SPxK_1 | 160 | 163 | PF00782 | 0.573 |
MOD_CDK_SPxK_1 | 157 | 163 | PF00069 | 0.577 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.267 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.669 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.531 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.669 |
MOD_CMANNOS | 76 | 79 | PF00535 | 0.527 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.737 |
MOD_Cter_Amidation | 62 | 65 | PF01082 | 0.495 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.729 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.304 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.728 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.416 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.689 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.267 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.642 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.520 |
MOD_LATS_1 | 201 | 207 | PF00433 | 0.349 |
MOD_LATS_1 | 305 | 311 | PF00433 | 0.708 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.585 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.556 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.295 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.442 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.347 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.363 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.555 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.497 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.558 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.242 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.457 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.620 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.479 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.566 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.506 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.540 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.201 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.339 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.705 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.569 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.408 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.417 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.514 |
MOD_SUMO_rev_2 | 3 | 11 | PF00179 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 309 | 314 | PF01217 | 0.632 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 51 | 55 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I045 | Leptomonas seymouri | 64% | 72% |
A0A0S4IVC3 | Bodo saltans | 49% | 94% |
A0A1X0NWZ9 | Trypanosomatidae | 57% | 89% |
A0A422MX57 | Trypanosoma rangeli | 55% | 90% |
A4HCU4 | Leishmania braziliensis | 84% | 81% |
C9ZV46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 89% |
E9AW89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5ARP5 | Trypanosoma cruzi | 56% | 89% |