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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A0A3S7XC14
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.698 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.411 |
CLV_TASPASE1 | 58 | 64 | PF01112 | 0.714 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.748 |
DEG_SPOP_SBC_1 | 281 | 285 | PF00917 | 0.772 |
DOC_CDC14_PxL_1 | 349 | 357 | PF14671 | 0.474 |
DOC_CYCLIN_RxL_1 | 50 | 60 | PF00134 | 0.590 |
DOC_MAPK_gen_1 | 293 | 303 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.531 |
DOC_MAPK_RevD_3 | 322 | 336 | PF00069 | 0.581 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.759 |
DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.513 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.711 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.752 |
LIG_CaM_IQ_9 | 253 | 269 | PF13499 | 0.634 |
LIG_CtBP_PxDLS_1 | 218 | 222 | PF00389 | 0.788 |
LIG_deltaCOP1_diTrp_1 | 101 | 107 | PF00928 | 0.722 |
LIG_deltaCOP1_diTrp_1 | 146 | 153 | PF00928 | 0.742 |
LIG_EH1_1 | 315 | 323 | PF00400 | 0.605 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.787 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.683 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.579 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.783 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.607 |
LIG_LIR_Apic_2 | 151 | 156 | PF02991 | 0.761 |
LIG_LIR_Gen_1 | 146 | 157 | PF02991 | 0.741 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 31 | 40 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.508 |
LIG_LYPXL_SIV_4 | 72 | 80 | PF13949 | 0.572 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.572 |
LIG_PDZ_Class_2 | 357 | 362 | PF00595 | 0.411 |
LIG_Pex14_1 | 149 | 153 | PF04695 | 0.766 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.576 |
LIG_SH2_GRB2like | 298 | 301 | PF00017 | 0.581 |
LIG_SH2_GRB2like | 47 | 50 | PF00017 | 0.619 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.659 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 343 | 346 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.606 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.765 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.726 |
LIG_SUMO_SIM_par_1 | 83 | 90 | PF11976 | 0.551 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.426 |
LIG_UBA3_1 | 94 | 100 | PF00899 | 0.584 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.651 |
MOD_CDK_SPK_2 | 322 | 327 | PF00069 | 0.492 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.716 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.785 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.684 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.472 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.707 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.602 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.504 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.639 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.771 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.622 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.716 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.696 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.587 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.679 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.579 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.754 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.700 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.597 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.634 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.609 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.696 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.618 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.537 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.640 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.714 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.702 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.690 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.515 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.488 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.438 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.548 |
MOD_OFUCOSY | 161 | 166 | PF10250 | 0.674 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.760 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.675 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.687 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.678 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.714 |
MOD_PKB_1 | 223 | 231 | PF00069 | 0.748 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.592 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.499 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.727 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.613 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.539 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.687 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.479 |
TRG_DiLeu_BaEn_1 | 90 | 95 | PF01217 | 0.561 |
TRG_DiLeu_BaEn_4 | 329 | 335 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 350 | 355 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.559 |
TRG_NES_CRM1_1 | 46 | 60 | PF08389 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I247 | Leptomonas seymouri | 40% | 100% |
A4HQD4 | Leishmania braziliensis | 62% | 100% |
A4IE26 | Leishmania infantum | 99% | 100% |
E9AU50 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q0E5 | Leishmania major | 91% | 100% |