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: E9APH8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.833 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.644 |
CLV_PCSK_FUR_1 | 480 | 484 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.572 |
CLV_Separin_Metazoa | 15 | 19 | PF03568 | 0.414 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.528 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.713 |
DOC_CKS1_1 | 393 | 398 | PF01111 | 0.728 |
DOC_CYCLIN_yCln2_LP_2 | 174 | 180 | PF00134 | 0.766 |
DOC_MAPK_DCC_7 | 385 | 393 | PF00069 | 0.530 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.768 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.616 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.628 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.719 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.468 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.765 |
LIG_14-3-3_CanoR_1 | 236 | 244 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 314 | 324 | PF00244 | 0.486 |
LIG_14-3-3_CterR_2 | 482 | 486 | PF00244 | 0.816 |
LIG_APCC_ABBA_1 | 203 | 208 | PF00400 | 0.699 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.668 |
LIG_Clathr_ClatBox_1 | 225 | 229 | PF01394 | 0.466 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.724 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.517 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.634 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.551 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.785 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.609 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.476 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.542 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.644 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.533 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.732 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.754 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.568 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.696 |
LIG_GBD_Chelix_1 | 226 | 234 | PF00786 | 0.571 |
LIG_GBD_Chelix_1 | 302 | 310 | PF00786 | 0.498 |
LIG_Integrin_RGD_1 | 99 | 101 | PF01839 | 0.531 |
LIG_LIR_Apic_2 | 166 | 172 | PF02991 | 0.723 |
LIG_LIR_Gen_1 | 150 | 160 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.396 |
LIG_LIR_LC3C_4 | 222 | 227 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.522 |
LIG_NRBOX | 461 | 467 | PF00104 | 0.644 |
LIG_PDZ_Class_1 | 481 | 486 | PF00595 | 0.819 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.399 |
LIG_Rb_pABgroove_1 | 147 | 155 | PF01858 | 0.703 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.573 |
LIG_SH2_CRK | 217 | 221 | PF00017 | 0.743 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.684 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.734 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.703 |
LIG_SH2_STAT3 | 337 | 340 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.344 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.753 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.713 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.499 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.423 |
LIG_SUMO_SIM_anti_2 | 222 | 229 | PF11976 | 0.414 |
LIG_SUMO_SIM_anti_2 | 420 | 429 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 103 | 110 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 222 | 229 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 420 | 429 | PF11976 | 0.535 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.659 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.759 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.643 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.709 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.350 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.515 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.498 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.754 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.654 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.515 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.528 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.732 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.724 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.622 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.660 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.690 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.660 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.768 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.525 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.587 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.814 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.523 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.675 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.571 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.598 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.791 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.662 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.706 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.474 |
MOD_N-GLC_2 | 371 | 373 | PF02516 | 0.643 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.665 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.421 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.579 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.682 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.830 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.754 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.403 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.568 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.623 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.599 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.484 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.713 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.570 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.499 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.455 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.558 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.677 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.532 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.707 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.367 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.750 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.524 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.539 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.731 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.770 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.655 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.479 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.516 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.723 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.610 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.762 |
TRG_DiLeu_BaEn_1 | 351 | 356 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.642 |
TRG_DiLeu_BaEn_2 | 18 | 24 | PF01217 | 0.599 |
TRG_DiLeu_BaEn_4 | 351 | 357 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 84 | 89 | PF01217 | 0.736 |
TRG_DiLeu_LyEn_5 | 351 | 356 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.744 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.681 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.688 |
TRG_NES_CRM1_1 | 147 | 161 | PF08389 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 256 | 261 | PF00026 | 0.600 |
TRG_PTS1 | 483 | 486 | PF00515 | 0.729 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K4 | Leptomonas seymouri | 48% | 83% |
A0A3S7WSN4 | Leishmania donovani | 88% | 100% |
A4H7E3 | Leishmania braziliensis | 73% | 100% |
A4HVT3 | Leishmania infantum | 88% | 100% |
Q4QG00 | Leishmania major | 88% | 100% |