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: A4H9C8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.400 |
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.389 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.396 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.578 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.389 |
DEG_MDM2_SWIB_1 | 28 | 36 | PF02201 | 0.227 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.562 |
DOC_CDC14_PxL_1 | 200 | 208 | PF14671 | 0.395 |
DOC_MAPK_gen_1 | 50 | 58 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 228 | 235 | PF00069 | 0.482 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.435 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.453 |
LIG_14-3-3_CanoR_1 | 132 | 139 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 261 | 270 | PF00244 | 0.385 |
LIG_Actin_WH2_1 | 196 | 212 | PF00022 | 0.391 |
LIG_Actin_WH2_2 | 68 | 83 | PF00022 | 0.439 |
LIG_BIR_III_4 | 165 | 169 | PF00653 | 0.396 |
LIG_BIR_III_4 | 221 | 225 | PF00653 | 0.402 |
LIG_CaM_NSCaTE_8 | 243 | 250 | PF13499 | 0.386 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.302 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.469 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.403 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.572 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.303 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.456 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.385 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.419 |
LIG_LIR_Apic_2 | 341 | 346 | PF02991 | 0.555 |
LIG_LIR_Apic_2 | 59 | 64 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 123 | 131 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 152 | 160 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 268 | 274 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 123 | 127 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.478 |
LIG_MAD2 | 196 | 204 | PF02301 | 0.490 |
LIG_MYND_3 | 203 | 207 | PF01753 | 0.393 |
LIG_NRBOX | 194 | 200 | PF00104 | 0.380 |
LIG_PCNA_yPIPBox_3 | 132 | 143 | PF02747 | 0.308 |
LIG_Pex14_1 | 115 | 119 | PF04695 | 0.378 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.227 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.438 |
LIG_SH2_PTP2 | 26 | 29 | PF00017 | 0.369 |
LIG_SH2_PTP2 | 331 | 334 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.220 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.395 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.290 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.384 |
LIG_SUMO_SIM_anti_2 | 16 | 21 | PF11976 | 0.227 |
LIG_SUMO_SIM_anti_2 | 387 | 394 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 76 | 81 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 86 | 91 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 15 | 21 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 172 | 179 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 196 | 202 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 54 | 59 | PF11976 | 0.374 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.466 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.403 |
LIG_TYR_ITIM | 24 | 29 | PF00017 | 0.292 |
LIG_UBA3_1 | 308 | 316 | PF00899 | 0.391 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.489 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.424 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.297 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.392 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.445 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.523 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.592 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.366 |
MOD_GlcNHglycan | 221 | 225 | PF01048 | 0.632 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.704 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.717 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.664 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.641 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.368 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.464 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.429 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.553 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.413 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.436 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.541 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.626 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.302 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.392 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.450 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.461 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.489 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.447 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.342 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.326 |
MOD_PK_1 | 145 | 151 | PF00069 | 0.316 |
MOD_PKA_1 | 241 | 247 | PF00069 | 0.468 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.469 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.405 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.407 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.414 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.404 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.359 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.379 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.392 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.417 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.462 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.340 |
TRG_DiLeu_BaEn_1 | 373 | 378 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 169 | 174 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.358 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 185 | 190 | PF00026 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 196 | 201 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 400 | 404 | PF00026 | 0.785 |
TRG_Pf-PMV_PEXEL_1 | 53 | 57 | PF00026 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P351 | Leptomonas seymouri | 28% | 100% |
A0A3S7WUS7 | Leishmania donovani | 64% | 100% |
A4HXQ0 | Leishmania infantum | 65% | 100% |
E9ARG1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q4QE18 | Leishmania major | 62% | 99% |