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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AYY5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.648 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.641 |
CLV_PCSK_FUR_1 | 397 | 401 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.789 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.510 |
DOC_CKS1_1 | 56 | 61 | PF01111 | 0.732 |
DOC_MAPK_gen_1 | 216 | 224 | PF00069 | 0.720 |
DOC_MAPK_gen_1 | 325 | 332 | PF00069 | 0.581 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.656 |
DOC_PP2B_LxvP_1 | 205 | 208 | PF13499 | 0.756 |
DOC_PP4_FxxP_1 | 328 | 331 | PF00568 | 0.584 |
DOC_SPAK_OSR1_1 | 327 | 331 | PF12202 | 0.571 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.754 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.758 |
LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 447 | 455 | PF00244 | 0.548 |
LIG_APCC_ABBA_1 | 302 | 307 | PF00400 | 0.759 |
LIG_APCC_ABBA_1 | 329 | 334 | PF00400 | 0.599 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.752 |
LIG_BRCT_BRCA1_1 | 285 | 289 | PF00533 | 0.590 |
LIG_BRCT_BRCA1_2 | 285 | 291 | PF00533 | 0.589 |
LIG_deltaCOP1_diTrp_1 | 176 | 182 | PF00928 | 0.445 |
LIG_EVH1_1 | 110 | 114 | PF00568 | 0.785 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.684 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.764 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.619 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.546 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.608 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.519 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.606 |
LIG_LIR_Apic_2 | 204 | 209 | PF02991 | 0.759 |
LIG_LIR_Apic_2 | 326 | 331 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.604 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.656 |
LIG_Pex14_2 | 328 | 332 | PF04695 | 0.581 |
LIG_Pex14_2 | 345 | 349 | PF04695 | 0.464 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.732 |
LIG_SH2_GRB2like | 348 | 351 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 306 | 310 | PF00017 | 0.522 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.759 |
LIG_SH2_STAP1 | 389 | 393 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.759 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.690 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.769 |
LIG_SH3_1 | 206 | 212 | PF00018 | 0.763 |
LIG_SH3_2 | 170 | 175 | PF14604 | 0.672 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.652 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.726 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.639 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.691 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.733 |
LIG_SUMO_SIM_par_1 | 100 | 109 | PF11976 | 0.669 |
LIG_SUMO_SIM_par_1 | 220 | 227 | PF11976 | 0.798 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.767 |
LIG_TYR_ITSM | 264 | 271 | PF00017 | 0.740 |
LIG_WW_3 | 112 | 116 | PF00397 | 0.705 |
LIG_WW_3 | 207 | 211 | PF00397 | 0.763 |
MOD_CDC14_SPxK_1 | 172 | 175 | PF00782 | 0.667 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.705 |
MOD_CDK_SPK_2 | 333 | 338 | PF00069 | 0.692 |
MOD_CDK_SPK_2 | 55 | 60 | PF00069 | 0.458 |
MOD_CDK_SPxK_1 | 169 | 175 | PF00069 | 0.676 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.770 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.774 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.759 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.579 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.535 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.771 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.796 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.612 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.698 |
MOD_Cter_Amidation | 311 | 314 | PF01082 | 0.687 |
MOD_DYRK1A_RPxSP_1 | 169 | 173 | PF00069 | 0.681 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.716 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.672 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.700 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.776 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.612 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.686 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.619 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.464 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.511 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.732 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.640 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.729 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.813 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.587 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.578 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.657 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.761 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.602 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.570 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.662 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.639 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.520 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.789 |
MOD_NEK2_2 | 263 | 268 | PF00069 | 0.744 |
MOD_OFUCOSY | 260 | 267 | PF10250 | 0.753 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.805 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.570 |
MOD_PKA_1 | 314 | 320 | PF00069 | 0.669 |
MOD_PKA_1 | 399 | 405 | PF00069 | 0.580 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.765 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.763 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.679 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.633 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.785 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.510 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.545 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.651 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.532 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.746 |
MOD_PKB_1 | 397 | 405 | PF00069 | 0.571 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.643 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.623 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.648 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.671 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.768 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.698 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.706 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.689 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.640 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.632 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.759 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 464 | 466 | PF00400 | 0.651 |
TRG_NLS_MonoExtC_3 | 298 | 303 | PF00514 | 0.692 |
TRG_NLS_MonoExtN_4 | 119 | 126 | PF00514 | 0.626 |
TRG_NLS_MonoExtN_4 | 297 | 304 | PF00514 | 0.691 |
TRG_NLS_MonoExtN_4 | 397 | 402 | PF00514 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 403 | 407 | PF00026 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4D2 | Leptomonas seymouri | 40% | 84% |
A0A3S7X0I5 | Leishmania donovani | 88% | 100% |
A4HFK5 | Leishmania braziliensis | 73% | 100% |
D0A5T1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AD60 | Leishmania major | 89% | 100% |
E9AHF5 | Leishmania infantum | 88% | 100% |