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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4QFY2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.757 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.392 |
DEG_SCF_FBW7_1 | 174 | 181 | PF00400 | 0.585 |
DEG_SCF_FBW7_1 | 226 | 233 | PF00400 | 0.495 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.595 |
DOC_CKS1_1 | 175 | 180 | PF01111 | 0.576 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.498 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.558 |
DOC_PP4_FxxP_1 | 227 | 230 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.715 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.730 |
LIG_Actin_WH2_2 | 104 | 122 | PF00022 | 0.380 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.526 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.540 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.544 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.503 |
LIG_LIR_Apic_2 | 225 | 230 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 218 | 227 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.649 |
LIG_PCNA_yPIPBox_3 | 8 | 17 | PF02747 | 0.656 |
LIG_Pex14_2 | 238 | 242 | PF04695 | 0.469 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.645 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.527 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.659 |
LIG_SH3_4 | 212 | 219 | PF00018 | 0.401 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.401 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.603 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.572 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.648 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.664 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.715 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.548 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.622 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.548 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.611 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.739 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.744 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.479 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.383 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.466 |
MOD_GlcNHglycan | 72 | 76 | PF01048 | 0.425 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.483 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.567 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.397 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.494 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.492 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.510 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.647 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.490 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.554 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.470 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.474 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.542 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.602 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.567 |
MOD_PK_1 | 58 | 64 | PF00069 | 0.694 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.724 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.587 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.509 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.500 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.557 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.540 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.429 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.607 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.564 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.498 |
MOD_SUMO_for_1 | 144 | 147 | PF00179 | 0.457 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.505 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.680 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.662 |
TRG_NLS_MonoExtC_3 | 141 | 147 | PF00514 | 0.560 |
TRG_NLS_MonoExtN_4 | 140 | 146 | PF00514 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 142 | 147 | PF00026 | 0.783 |
TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXV2 | Leptomonas seymouri | 50% | 100% |
A0A0S4IQN6 | Bodo saltans | 25% | 97% |
A0A1X0NNV6 | Trypanosomatidae | 24% | 100% |
A0A3S5H6Q5 | Leishmania donovani | 90% | 100% |
A0A422NXF3 | Trypanosoma rangeli | 25% | 100% |
A4H7G4 | Leishmania braziliensis | 71% | 100% |
A4HVU5 | Leishmania infantum | 90% | 100% |
E9APJ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |