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: A0A3S7WY45
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.769 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.760 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.557 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.713 |
DOC_CDC14_PxL_1 | 258 | 266 | PF14671 | 0.608 |
DOC_CKS1_1 | 284 | 289 | PF01111 | 0.741 |
DOC_MAPK_gen_1 | 230 | 239 | PF00069 | 0.744 |
DOC_MAPK_gen_1 | 64 | 71 | PF00069 | 0.665 |
DOC_MAPK_MEF2A_6 | 361 | 370 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 64 | 71 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 95 | 103 | PF00069 | 0.484 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.763 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.821 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 119 | 124 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.830 |
LIG_14-3-3_CanoR_1 | 355 | 364 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 385 | 394 | PF00244 | 0.786 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.626 |
LIG_Actin_WH2_2 | 54 | 72 | PF00022 | 0.581 |
LIG_APCC_ABBA_1 | 97 | 102 | PF00400 | 0.617 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.712 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.676 |
LIG_BRCT_BRCA1_1 | 398 | 402 | PF00533 | 0.593 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.603 |
LIG_DLG_GKlike_1 | 373 | 381 | PF00625 | 0.733 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.612 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.517 |
LIG_LIR_Apic_2 | 199 | 205 | PF02991 | 0.782 |
LIG_LIR_Apic_2 | 274 | 279 | PF02991 | 0.682 |
LIG_LIR_Apic_2 | 294 | 299 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.649 |
LIG_MLH1_MIPbox_1 | 249 | 253 | PF16413 | 0.576 |
LIG_MYND_1 | 382 | 386 | PF01753 | 0.537 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.780 |
LIG_SH2_NCK_1 | 175 | 179 | PF00017 | 0.696 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.771 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.669 |
LIG_SH3_1 | 328 | 334 | PF00018 | 0.748 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.727 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.578 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.742 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.613 |
LIG_SUMO_SIM_anti_2 | 42 | 47 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 42 | 47 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 57 | 63 | PF11976 | 0.611 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.544 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.745 |
LIG_WW_3 | 297 | 301 | PF00397 | 0.607 |
MOD_CDK_SPxK_1 | 294 | 300 | PF00069 | 0.783 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.718 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.598 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.737 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.807 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.706 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.747 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.543 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.843 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.722 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.789 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.638 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.579 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.672 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.708 |
MOD_GlcNHglycan | 304 | 308 | PF01048 | 0.783 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.669 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.725 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.634 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.716 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.658 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.582 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.811 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.690 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.788 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.706 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.719 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.850 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.734 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.759 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.510 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.777 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.788 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.783 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.758 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.542 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.394 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.621 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.606 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.686 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.490 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.734 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.527 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.648 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.708 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.830 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.671 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.675 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.661 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.708 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.726 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.774 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.770 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.715 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.697 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 327 | 329 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.784 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEP2 | Leptomonas seymouri | 36% | 100% |
A4HDU6 | Leishmania braziliensis | 61% | 100% |
A4I0N7 | Leishmania infantum | 98% | 100% |
E9AWN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QAT4 | Leishmania major | 88% | 100% |