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 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AQJ7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.441 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.415 |
CLV_PCSK_PC7_1 | 16 | 22 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.249 |
DEG_APCC_DBOX_1 | 15 | 23 | PF00400 | 0.600 |
DEG_APCC_DBOX_1 | 161 | 169 | PF00400 | 0.445 |
DEG_SPOP_SBC_1 | 232 | 236 | PF00917 | 0.510 |
DOC_CYCLIN_RxL_1 | 20 | 31 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 295 | 301 | PF00134 | 0.575 |
DOC_MAPK_gen_1 | 20 | 30 | PF00069 | 0.617 |
DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 291 | 299 | PF00069 | 0.462 |
DOC_MAPK_JIP1_4 | 291 | 297 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 291 | 299 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 323 | 332 | PF00069 | 0.372 |
DOC_PP1_RVXF_1 | 175 | 181 | PF00149 | 0.520 |
DOC_PP2B_LxvP_1 | 295 | 298 | PF13499 | 0.469 |
DOC_SPAK_OSR1_1 | 308 | 312 | PF12202 | 0.454 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.513 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 101 | 108 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 177 | 181 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 47 | 51 | PF00244 | 0.544 |
LIG_AP2alpha_2 | 282 | 284 | PF02296 | 0.517 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.443 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.464 |
LIG_CaMK_CASK_1 | 248 | 253 | PF00069 | 0.580 |
LIG_eIF4E_1 | 331 | 337 | PF01652 | 0.424 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.477 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.423 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.579 |
LIG_LIR_Apic_2 | 300 | 305 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.525 |
LIG_Pex14_1 | 334 | 338 | PF04695 | 0.411 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.542 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.442 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.585 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 345 | 349 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 108 | 112 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.594 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.460 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.526 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.400 |
LIG_TYR_ITIM | 339 | 344 | PF00017 | 0.400 |
MOD_CDK_SPxxK_3 | 212 | 219 | PF00069 | 0.609 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.502 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.401 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.491 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.596 |
MOD_CMANNOS | 71 | 74 | PF00535 | 0.745 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.821 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.805 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.713 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.424 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.742 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.461 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.439 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.372 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.536 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.643 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.452 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.408 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.432 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.563 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.319 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.545 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.469 |
MOD_NEK2_2 | 38 | 43 | PF00069 | 0.513 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.492 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.482 |
MOD_PK_1 | 196 | 202 | PF00069 | 0.528 |
MOD_PK_1 | 293 | 299 | PF00069 | 0.490 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.528 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.505 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.615 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.449 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.520 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.559 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.547 |
MOD_PKB_1 | 291 | 299 | PF00069 | 0.462 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.523 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.520 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.465 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.386 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.454 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.499 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.432 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.464 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.448 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.604 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 356 | 361 | PF00179 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.734 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0F8 | Leptomonas seymouri | 41% | 95% |
A0A3S7WTU6 | Leishmania donovani | 90% | 100% |
A4H8G5 | Leishmania braziliensis | 62% | 100% |
E9AGN1 | Leishmania infantum | 90% | 100% |
Q4QEY0 | Leishmania major | 83% | 100% |