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 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031965 | nuclear membrane | 4 | 1 |
Related structures:
AlphaFold database: E9B5W4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.651 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.527 |
DEG_COP1_1 | 393 | 400 | PF00400 | 0.496 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.529 |
DEG_SPOP_SBC_1 | 106 | 110 | PF00917 | 0.661 |
DOC_CKS1_1 | 121 | 126 | PF01111 | 0.633 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 276 | 282 | PF00134 | 0.411 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.474 |
DOC_PP2B_LxvP_1 | 275 | 278 | PF13499 | 0.513 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.701 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.652 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.774 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 156 | 163 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.466 |
LIG_14-3-3_CterR_2 | 421 | 424 | PF00244 | 0.540 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.723 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.708 |
LIG_Clathr_ClatBox_1 | 389 | 393 | PF01394 | 0.513 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.635 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.466 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.494 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.377 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.509 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.511 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.411 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.246 |
LIG_GBD_Chelix_1 | 309 | 317 | PF00786 | 0.751 |
LIG_GBD_Chelix_1 | 384 | 392 | PF00786 | 0.402 |
LIG_LIR_Apic_2 | 229 | 235 | PF02991 | 0.705 |
LIG_LIR_Apic_2 | 80 | 86 | PF02991 | 0.703 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.695 |
LIG_LIR_Gen_1 | 266 | 276 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 355 | 363 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 386 | 395 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.725 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 355 | 359 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 95 | 99 | PF02991 | 0.711 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.759 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.769 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.222 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.645 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.692 |
LIG_SH2_STAP1 | 19 | 23 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.732 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.710 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.472 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.829 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.608 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.684 |
LIG_SUMO_SIM_anti_2 | 381 | 386 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 4 | 11 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 386 | 394 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 408 | 413 | PF11976 | 0.249 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.815 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.705 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.688 |
LIG_TRAF2_2 | 124 | 129 | PF00917 | 0.628 |
LIG_TRFH_1 | 33 | 37 | PF08558 | 0.622 |
LIG_WRC_WIRS_1 | 384 | 389 | PF05994 | 0.513 |
MOD_CDC14_SPxK_1 | 110 | 113 | PF00782 | 0.613 |
MOD_CDK_SPxK_1 | 107 | 113 | PF00069 | 0.611 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.746 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.836 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.778 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.488 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.500 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.465 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.739 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.713 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.632 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.551 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.506 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.495 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.592 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.411 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.569 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.766 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.720 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.778 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.695 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.508 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.569 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.510 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.381 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.696 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.708 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.553 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.605 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.715 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.715 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.551 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.588 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.433 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.661 |
MOD_NEK2_2 | 398 | 403 | PF00069 | 0.228 |
MOD_OFUCOSY | 364 | 370 | PF10250 | 0.411 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.777 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.704 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.713 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.773 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.721 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.577 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.546 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.730 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.712 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.651 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.513 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.211 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.767 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.445 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.405 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.513 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.332 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.742 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.770 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.779 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.800 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.499 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.505 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.727 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.773 |
MOD_SUMO_rev_2 | 293 | 303 | PF00179 | 0.405 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.728 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHG2 | Leptomonas seymouri | 46% | 99% |
A0A3Q8IP51 | Leishmania donovani | 87% | 100% |
A4HMB5 | Leishmania braziliensis | 68% | 96% |
A4IAY1 | Leishmania infantum | 87% | 100% |
E9AEQ9 | Leishmania major | 88% | 100% |