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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HNM0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.718 |
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.223 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.531 |
CLV_PCSK_FUR_1 | 118 | 122 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.460 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.385 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.453 |
DOC_MAPK_gen_1 | 120 | 130 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 174 | 181 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 305 | 311 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 355 | 364 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 174 | 181 | PF00069 | 0.457 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.668 |
DOC_USP7_MATH_2 | 23 | 29 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 174 | 178 | PF12436 | 0.483 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.385 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 231 | 240 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 51 | 58 | PF00244 | 0.589 |
LIG_Actin_WH2_2 | 342 | 360 | PF00022 | 0.384 |
LIG_AP2alpha_2 | 300 | 302 | PF02296 | 0.449 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.683 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.449 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.404 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.333 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.537 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.446 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.503 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.568 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.356 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.352 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.552 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.448 |
LIG_PCNA_PIPBox_1 | 252 | 261 | PF02747 | 0.625 |
LIG_PCNA_yPIPBox_3 | 250 | 259 | PF02747 | 0.506 |
LIG_RPA_C_Fungi | 207 | 219 | PF08784 | 0.616 |
LIG_RPA_C_Fungi | 46 | 58 | PF08784 | 0.326 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.511 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.756 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.743 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.469 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.744 |
MOD_CDK_SPxxK_3 | 275 | 282 | PF00069 | 0.407 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.634 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.639 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.223 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.425 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.524 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.649 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.567 |
MOD_Cter_Amidation | 140 | 143 | PF01082 | 0.528 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.631 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.651 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.422 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.425 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.657 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.691 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.583 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.343 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.343 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.388 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.413 |
MOD_OFUCOSY | 66 | 72 | PF10250 | 0.447 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.652 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.387 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.458 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.385 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.636 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.449 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.449 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.730 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.663 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.479 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.433 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.340 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.430 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.418 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.533 |
MOD_SUMO_for_1 | 147 | 150 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 105 | 113 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 15 | 20 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_4 | 125 | 131 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.475 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.569 |
TRG_NES_CRM1_1 | 150 | 162 | PF08389 | 0.541 |
TRG_NLS_Bipartite_1 | 156 | 178 | PF00514 | 0.538 |
TRG_NLS_MonoExtC_3 | 173 | 178 | PF00514 | 0.482 |
TRG_NLS_MonoExtC_3 | 274 | 279 | PF00514 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I208 | Leptomonas seymouri | 62% | 99% |
A0A0S4JLL2 | Bodo saltans | 37% | 94% |
A0A1X0P8K7 | Trypanosomatidae | 48% | 100% |
A0A3S5IQV7 | Trypanosoma rangeli | 47% | 100% |
A0A3S7XA96 | Leishmania donovani | 78% | 100% |
A4ICX4 | Leishmania infantum | 77% | 100% |
D0A2H5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 89% |
E9ASD1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q265 | Leishmania major | 78% | 100% |
V5BQK6 | Trypanosoma cruzi | 43% | 100% |