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: A4I1N5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.480 |
CLV_PCSK_FUR_1 | 393 | 397 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.598 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.460 |
DOC_CDC14_PxL_1 | 70 | 78 | PF14671 | 0.518 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.434 |
DOC_MAPK_gen_1 | 209 | 218 | PF00069 | 0.656 |
DOC_MIT_MIM_1 | 388 | 397 | PF04212 | 0.599 |
DOC_PP1_RVXF_1 | 112 | 118 | PF00149 | 0.527 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.519 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.484 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.839 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 101 | 108 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 431 | 437 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 49 | 53 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.546 |
LIG_Clathr_ClatBox_1 | 130 | 134 | PF01394 | 0.659 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.715 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.714 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.715 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.538 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.789 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.503 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.725 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.476 |
LIG_LYPXL_S_1 | 72 | 76 | PF13949 | 0.520 |
LIG_LYPXL_yS_3 | 73 | 76 | PF13949 | 0.523 |
LIG_NRBOX | 393 | 399 | PF00104 | 0.606 |
LIG_RPA_C_Fungi | 147 | 159 | PF08784 | 0.629 |
LIG_RPA_C_Fungi | 196 | 208 | PF08784 | 0.611 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.703 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.559 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.481 |
LIG_SH2_SRC | 371 | 374 | PF00017 | 0.664 |
LIG_SH2_SRC | 400 | 403 | PF00017 | 0.728 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 466 | 470 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.524 |
LIG_SH3_1 | 258 | 264 | PF00018 | 0.788 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.453 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.780 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.774 |
LIG_SUMO_SIM_anti_2 | 129 | 134 | PF11976 | 0.662 |
LIG_SUMO_SIM_anti_2 | 440 | 445 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 129 | 134 | PF11976 | 0.601 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.714 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.582 |
LIG_WW_3 | 306 | 310 | PF00397 | 0.618 |
MOD_CDC14_SPxK_1 | 111 | 114 | PF00782 | 0.491 |
MOD_CDC14_SPxK_1 | 306 | 309 | PF00782 | 0.662 |
MOD_CDC14_SPxK_1 | 89 | 92 | PF00782 | 0.477 |
MOD_CDK_SPK_2 | 13 | 18 | PF00069 | 0.443 |
MOD_CDK_SPK_2 | 86 | 91 | PF00069 | 0.483 |
MOD_CDK_SPxK_1 | 108 | 114 | PF00069 | 0.499 |
MOD_CDK_SPxK_1 | 303 | 309 | PF00069 | 0.808 |
MOD_CDK_SPxK_1 | 86 | 92 | PF00069 | 0.482 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.676 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.478 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.675 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.714 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.447 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.792 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.447 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.557 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.504 |
MOD_Cter_Amidation | 36 | 39 | PF01082 | 0.444 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.667 |
MOD_GlcNHglycan | 247 | 251 | PF01048 | 0.667 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.678 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.589 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.384 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.477 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.759 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.622 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.595 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.763 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.533 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.464 |
MOD_LATS_1 | 252 | 258 | PF00433 | 0.727 |
MOD_LATS_1 | 99 | 105 | PF00433 | 0.495 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.751 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.600 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.465 |
MOD_NEK2_2 | 68 | 73 | PF00069 | 0.464 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.551 |
MOD_PIKK_1 | 284 | 290 | PF00454 | 0.772 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.470 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.455 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.700 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.516 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.532 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.748 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.675 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.455 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.472 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.508 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.484 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.724 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.840 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.595 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.690 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.699 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 144 | 149 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.711 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1G6 | Leptomonas seymouri | 37% | 100% |
A0A3Q8IDF4 | Leishmania donovani | 99% | 100% |
A4HE89 | Leishmania braziliensis | 73% | 100% |
E9AXR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q9Q2 | Leishmania major | 86% | 100% |