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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HNH9
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005525 | GTP binding | 5 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0019001 | guanyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.443 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.634 |
DEG_SPOP_SBC_1 | 38 | 42 | PF00917 | 0.463 |
DOC_CKS1_1 | 159 | 164 | PF01111 | 0.330 |
DOC_CKS1_1 | 70 | 75 | PF01111 | 0.639 |
DOC_CYCLIN_RxL_1 | 108 | 117 | PF00134 | 0.469 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 323 | 332 | PF00069 | 0.361 |
DOC_MAPK_gen_1 | 94 | 101 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 331 | 340 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 298 | 304 | PF00149 | 0.306 |
DOC_PP2B_LxvP_1 | 104 | 107 | PF13499 | 0.478 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.532 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.420 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.708 |
LIG_14-3-3_CanoR_1 | 236 | 244 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 26 | 33 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 53 | 62 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.571 |
LIG_APCC_ABBA_1 | 330 | 335 | PF00400 | 0.352 |
LIG_BIR_III_2 | 263 | 267 | PF00653 | 0.384 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.225 |
LIG_deltaCOP1_diTrp_1 | 223 | 233 | PF00928 | 0.372 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.402 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.349 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.503 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.451 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.526 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.432 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.620 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.406 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.374 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.441 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.375 |
LIG_LIR_Apic_2 | 4 | 10 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 153 | 162 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.307 |
LIG_MLH1_MIPbox_1 | 264 | 268 | PF16413 | 0.225 |
LIG_Pex14_1 | 233 | 237 | PF04695 | 0.447 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.432 |
LIG_SH2_STAT3 | 88 | 91 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.318 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.448 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.394 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.390 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.239 |
LIG_SUMO_SIM_par_1 | 315 | 322 | PF11976 | 0.511 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.621 |
MOD_CDK_SPK_2 | 69 | 74 | PF00069 | 0.641 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.580 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.520 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.406 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.295 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.462 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.656 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.700 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.528 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.707 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.638 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.358 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.671 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.721 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.759 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.481 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.571 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.537 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.687 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.709 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.725 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.550 |
MOD_LATS_1 | 51 | 57 | PF00433 | 0.648 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.561 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.424 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.377 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.459 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.452 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.350 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.376 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.479 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.553 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.493 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.447 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.656 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.323 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.701 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.601 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.359 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.624 |
MOD_PKB_1 | 234 | 242 | PF00069 | 0.293 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.607 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.407 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.342 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.414 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.496 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.432 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.362 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.364 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.677 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.706 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 60 | 63 | PF00400 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 258 | 263 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5M5 | Leptomonas seymouri | 61% | 90% |
A0A0S4JLN7 | Bodo saltans | 36% | 92% |
A0A1X0P4S5 | Trypanosomatidae | 55% | 92% |
A0A3Q8IFN6 | Leishmania donovani | 78% | 89% |
A0A422NCK5 | Trypanosoma rangeli | 50% | 100% |
A4IC35 | Leishmania infantum | 81% | 100% |
C9ZYD6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 98% |
E9AFZ0 | Leishmania major | 79% | 100% |
E9B743 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 89% |
V5B8T8 | Trypanosoma cruzi | 53% | 95% |