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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HMC4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 207 | 209 | PF00082 | 0.433 |
CLV_PCSK_PC7_1 | 204 | 210 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.427 |
CLV_Separin_Metazoa | 160 | 164 | PF03568 | 0.620 |
DOC_MAPK_MEF2A_6 | 67 | 76 | PF00069 | 0.599 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.784 |
DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.648 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 30 | 34 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 50 | 57 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 6 | 15 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 99 | 107 | PF00244 | 0.699 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.388 |
LIG_deltaCOP1_diTrp_1 | 215 | 220 | PF00928 | 0.681 |
LIG_eIF4E_1 | 217 | 223 | PF01652 | 0.438 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.534 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.358 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.629 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.636 |
LIG_LIR_Gen_1 | 219 | 227 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 170 | 174 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.694 |
LIG_Pex14_1 | 216 | 220 | PF04695 | 0.515 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.602 |
LIG_REV1ctd_RIR_1 | 237 | 241 | PF16727 | 0.531 |
LIG_RPA_C_Fungi | 143 | 155 | PF08784 | 0.385 |
LIG_SH2_STAT3 | 139 | 142 | PF00017 | 0.519 |
LIG_SUMO_SIM_anti_2 | 158 | 163 | PF11976 | 0.506 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.533 |
LIG_TRFH_1 | 37 | 41 | PF08558 | 0.535 |
LIG_UBA3_1 | 233 | 241 | PF00899 | 0.388 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.361 |
MOD_CDK_SPK_2 | 94 | 99 | PF00069 | 0.543 |
MOD_CDK_SPxxK_3 | 43 | 50 | PF00069 | 0.517 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.700 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.547 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.592 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.655 |
MOD_DYRK1A_RPxSP_1 | 164 | 168 | PF00069 | 0.520 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.653 |
MOD_GlcNHglycan | 149 | 153 | PF01048 | 0.439 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.602 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.676 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.673 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.572 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.339 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.588 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.568 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.603 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.764 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.711 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.609 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.559 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.348 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.466 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.552 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.578 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.581 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.253 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.490 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.444 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.379 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.515 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.540 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.463 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.388 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.284 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.490 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.517 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.541 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.527 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.647 |
MOD_SUMO_for_1 | 186 | 189 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 188 | 193 | PF00179 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 44 | 49 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.511 |
TRG_NLS_MonoCore_2 | 205 | 210 | PF00514 | 0.526 |
TRG_NLS_MonoExtN_4 | 204 | 211 | PF00514 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IV31 | Leishmania donovani | 75% | 100% |
A4IAZ0 | Leishmania infantum | 76% | 100% |
E9AER8 | Leishmania major | 78% | 100% |
E9B5X3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |