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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HUN5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.300 |
CLV_Separin_Metazoa | 121 | 125 | PF03568 | 0.665 |
DOC_ANK_TNKS_1 | 96 | 103 | PF00023 | 0.642 |
DOC_MAPK_MEF2A_6 | 23 | 32 | PF00069 | 0.507 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.645 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 19 | 23 | PF12436 | 0.533 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.675 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.541 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.680 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.642 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.580 |
LIG_Clathr_ClatBox_1 | 147 | 151 | PF01394 | 0.476 |
LIG_deltaCOP1_diTrp_1 | 246 | 250 | PF00928 | 0.487 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.585 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.476 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.603 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.493 |
LIG_LIR_Gen_1 | 173 | 180 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 226 | 237 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 246 | 255 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 34 | 43 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 34 | 38 | PF02991 | 0.534 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.467 |
LIG_SH2_NCK_1 | 47 | 51 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.390 |
LIG_SUMO_SIM_anti_2 | 143 | 149 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 146 | 151 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 75 | 80 | PF11976 | 0.480 |
LIG_WRC_WIRS_1 | 32 | 37 | PF05994 | 0.542 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.671 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.598 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.417 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.580 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.559 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.637 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.600 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.541 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.488 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.316 |
MOD_GlcNHglycan | 257 | 261 | PF01048 | 0.366 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.359 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.666 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.653 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.580 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.600 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.287 |
MOD_N-GLC_2 | 254 | 256 | PF02516 | 0.287 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.685 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.534 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.479 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.556 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.740 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.580 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.673 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.583 |
MOD_PK_1 | 124 | 130 | PF00069 | 0.535 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.541 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.371 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.580 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.580 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.555 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.500 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.517 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.458 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.406 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.547 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.543 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.721 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.675 |
MOD_SUMO_for_1 | 199 | 202 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 58 | 63 | PF00179 | 0.663 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.487 |
TRG_DiLeu_BaEn_2 | 222 | 228 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_3 | 239 | 245 | PF01217 | 0.500 |
TRG_DiLeu_LyEn_5 | 202 | 207 | PF01217 | 0.537 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HX75 | Leptomonas seymouri | 76% | 100% |
A0A0S4KKL7 | Bodo saltans | 29% | 87% |
A0A1X0NS45 | Trypanosomatidae | 37% | 100% |
A0A3Q8IB48 | Leishmania donovani | 100% | 100% |
A0A422NBS9 | Trypanosoma rangeli | 41% | 99% |
A4H6B1 | Leishmania braziliensis | 93% | 100% |
C9ZVR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AND3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
Q4QH91 | Leishmania major | 97% | 100% |
V5B466 | Trypanosoma cruzi | 41% | 88% |