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: A4H8V1
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.462 |
CLV_PCSK_FUR_1 | 80 | 84 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.399 |
CLV_PCSK_PC7_1 | 218 | 224 | PF00082 | 0.589 |
CLV_PCSK_PC7_1 | 80 | 86 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.477 |
DOC_CYCLIN_RxL_1 | 13 | 24 | PF00134 | 0.561 |
DOC_CYCLIN_RxL_1 | 92 | 101 | PF00134 | 0.505 |
DOC_MAPK_MEF2A_6 | 194 | 201 | PF00069 | 0.553 |
DOC_PP1_RVXF_1 | 14 | 21 | PF00149 | 0.547 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.469 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.529 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 148 | 153 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.562 |
LIG_BRCT_BRCA1_1 | 48 | 52 | PF00533 | 0.536 |
LIG_CtBP_PxDLS_1 | 28 | 32 | PF00389 | 0.345 |
LIG_deltaCOP1_diTrp_1 | 41 | 51 | PF00928 | 0.429 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.561 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.757 |
LIG_LIR_Gen_1 | 114 | 122 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 49 | 56 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.473 |
LIG_PTB_Apo_2 | 31 | 38 | PF02174 | 0.496 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.508 |
LIG_SH2_STAT3 | 40 | 43 | PF00017 | 0.518 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.538 |
LIG_WRC_WIRS_1 | 47 | 52 | PF05994 | 0.529 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.417 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.714 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.765 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.515 |
MOD_Cter_Amidation | 14 | 17 | PF01082 | 0.602 |
MOD_Cter_Amidation | 220 | 223 | PF01082 | 0.352 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.627 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.568 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.370 |
MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.778 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.448 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.342 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.765 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.633 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.502 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.473 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.367 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.543 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.641 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.382 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.516 |
MOD_Plk_2-3 | 186 | 192 | PF00069 | 0.534 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.468 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.536 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.536 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.467 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.543 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.466 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.436 |
TRG_NLS_Bipartite_1 | 79 | 98 | PF00514 | 0.462 |
TRG_NLS_MonoCore_2 | 91 | 96 | PF00514 | 0.498 |
TRG_NLS_MonoExtC_3 | 78 | 83 | PF00514 | 0.481 |
TRG_NLS_MonoExtC_3 | 91 | 96 | PF00514 | 0.459 |
TRG_NLS_MonoExtN_4 | 92 | 98 | PF00514 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 153 | 157 | PF00026 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 223 | 227 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 54 | 58 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I083 | Leptomonas seymouri | 58% | 95% |
A0A1X0NT13 | Trypanosomatidae | 45% | 94% |
A0A3R7KLV2 | Trypanosoma rangeli | 44% | 90% |
A0A3S5H6Z6 | Leishmania donovani | 75% | 98% |
A4HX70 | Leishmania infantum | 75% | 98% |
C9ZTU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9ARC7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QEJ3 | Leishmania major | 77% | 100% |