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: E9ALZ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.699 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.560 |
CLV_PCSK_PC7_1 | 196 | 202 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.629 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.553 |
DEG_SCF_TRCP1_1 | 105 | 111 | PF00400 | 0.385 |
DEG_SPOP_SBC_1 | 20 | 24 | PF00917 | 0.811 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.539 |
DOC_CKS1_1 | 400 | 405 | PF01111 | 0.809 |
DOC_CYCLIN_RxL_1 | 359 | 369 | PF00134 | 0.682 |
DOC_MAPK_DCC_7 | 311 | 320 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 84 | 93 | PF00069 | 0.486 |
DOC_PP1_RVXF_1 | 360 | 367 | PF00149 | 0.781 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.779 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.667 |
DOC_PP2B_LxvP_1 | 460 | 463 | PF13499 | 0.489 |
DOC_SPAK_OSR1_1 | 286 | 290 | PF12202 | 0.534 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.681 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.801 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 362 | 367 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 54 | 63 | PF00244 | 0.701 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.523 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.626 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.627 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.695 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.619 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.518 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.797 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.568 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.708 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.680 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.478 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.499 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.783 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.775 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.492 |
LIG_MYND_3 | 11 | 15 | PF01753 | 0.532 |
LIG_PDZ_Class_2 | 463 | 468 | PF00595 | 0.486 |
LIG_RPA_C_Fungi | 281 | 293 | PF08784 | 0.560 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.536 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.506 |
LIG_SH2_NCK_1 | 227 | 231 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.506 |
LIG_SH2_NCK_1 | 44 | 48 | PF00017 | 0.667 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 351 | 354 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.509 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.702 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.710 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.725 |
LIG_SUMO_SIM_par_1 | 432 | 438 | PF11976 | 0.438 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.636 |
LIG_WW_3 | 229 | 233 | PF00397 | 0.536 |
MOD_CDK_SPxK_1 | 226 | 232 | PF00069 | 0.535 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.598 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.709 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.666 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.723 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.821 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.462 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.629 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.604 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.782 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.738 |
MOD_DYRK1A_RPxSP_1 | 293 | 297 | PF00069 | 0.689 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.420 |
MOD_GlcNHglycan | 212 | 216 | PF01048 | 0.752 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.804 |
MOD_GlcNHglycan | 251 | 255 | PF01048 | 0.391 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.631 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.718 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.593 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.538 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.822 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.759 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.697 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.647 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.579 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.485 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.794 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.522 |
MOD_N-GLC_2 | 242 | 244 | PF02516 | 0.650 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.442 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.582 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.604 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.468 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.515 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.517 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.746 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.654 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.716 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.584 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.697 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.669 |
MOD_PKB_1 | 148 | 156 | PF00069 | 0.480 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.737 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.505 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.776 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.536 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.468 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.735 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.602 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.782 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.571 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.596 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.531 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.742 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.811 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.738 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.666 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.683 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.563 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.732 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.525 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.799 |
TRG_DiLeu_BaLyEn_6 | 221 | 226 | PF01217 | 0.722 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.531 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.731 |
TRG_Pf-PMV_PEXEL_1 | 126 | 131 | PF00026 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I162 | Leptomonas seymouri | 43% | 74% |
A0A3Q8IR74 | Leishmania donovani | 86% | 100% |
E9ADT9 | Leishmania major | 86% | 100% |
E9AHI3 | Leishmania infantum | 86% | 100% |
E9AIT6 | Leishmania braziliensis | 72% | 100% |