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 |
Related structures:
AlphaFold database: E9ALX6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.642 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.595 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.531 |
DOC_CKS1_1 | 317 | 322 | PF01111 | 0.654 |
DOC_CKS1_1 | 418 | 423 | PF01111 | 0.650 |
DOC_MAPK_gen_1 | 38 | 45 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 39 | 46 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.634 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.650 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.806 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.655 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 124 | 133 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 409 | 418 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 424 | 432 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.583 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.618 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.627 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.675 |
LIG_deltaCOP1_diTrp_1 | 77 | 82 | PF00928 | 0.631 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.623 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.599 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.682 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.700 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.716 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.670 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.620 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.739 |
LIG_GBD_Chelix_1 | 43 | 51 | PF00786 | 0.634 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 396 | 400 | PF02991 | 0.650 |
LIG_MYND_1 | 214 | 218 | PF01753 | 0.601 |
LIG_REV1ctd_RIR_1 | 43 | 53 | PF16727 | 0.458 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.662 |
LIG_SH2_NCK_1 | 111 | 115 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 111 | 115 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.471 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.625 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.563 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.623 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.672 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.656 |
LIG_TRAF2_1 | 75 | 78 | PF00917 | 0.634 |
LIG_TRAF2_2 | 358 | 363 | PF00917 | 0.627 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.489 |
MOD_CDC14_SPxK_1 | 283 | 286 | PF00782 | 0.663 |
MOD_CDC14_SPxK_1 | 326 | 329 | PF00782 | 0.771 |
MOD_CDK_SPK_2 | 336 | 341 | PF00069 | 0.673 |
MOD_CDK_SPxK_1 | 280 | 286 | PF00069 | 0.667 |
MOD_CDK_SPxK_1 | 323 | 329 | PF00069 | 0.807 |
MOD_CDK_SPxxK_3 | 417 | 424 | PF00069 | 0.691 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.618 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.574 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.565 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.612 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.735 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.700 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.727 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.634 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.590 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.736 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.750 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.677 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.622 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.729 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.553 |
MOD_Cter_Amidation | 36 | 39 | PF01082 | 0.468 |
MOD_Cter_Amidation | 65 | 68 | PF01082 | 0.641 |
MOD_DYRK1A_RPxSP_1 | 200 | 204 | PF00069 | 0.580 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.682 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.491 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.550 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.606 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.720 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.608 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.546 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.593 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.620 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.711 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.627 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.720 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.584 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.623 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.558 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.649 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.580 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.697 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.574 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.609 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.694 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.661 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.678 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.639 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.657 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.753 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.701 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.602 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.616 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.649 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.626 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.680 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.667 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.673 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.662 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.714 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.756 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.630 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.638 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.822 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.485 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.742 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.622 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.640 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.668 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.571 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.721 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.583 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.773 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.610 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.682 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.648 |
MOD_SUMO_rev_2 | 48 | 54 | PF00179 | 0.663 |
TRG_DiLeu_BaLyEn_6 | 215 | 220 | PF01217 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.634 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 432 | 435 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 91 | 94 | PF00400 | 0.476 |
TRG_NLS_MonoCore_2 | 37 | 42 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 237 | 242 | PF00026 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.668 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8D7 | Leptomonas seymouri | 39% | 100% |
A0A3Q8IFA6 | Leishmania donovani | 89% | 100% |
A4HHA8 | Leishmania braziliensis | 69% | 99% |
A4I4F4 | Leishmania infantum | 88% | 100% |
E9ADV4 | Leishmania major | 88% | 100% |