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: A0A3S7WR94
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.669 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.575 |
CLV_PCSK_FUR_1 | 115 | 119 | PF00082 | 0.600 |
CLV_PCSK_FUR_1 | 311 | 315 | PF00082 | 0.631 |
CLV_PCSK_FUR_1 | 79 | 83 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.793 |
CLV_PCSK_PC7_1 | 113 | 119 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.794 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.781 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.625 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.544 |
DEG_Kelch_Keap1_1 | 207 | 212 | PF01344 | 0.781 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.807 |
DOC_CYCLIN_RxL_1 | 178 | 186 | PF00134 | 0.588 |
DOC_CYCLIN_yCln2_LP_2 | 123 | 129 | PF00134 | 0.636 |
DOC_CYCLIN_yCln2_LP_2 | 371 | 374 | PF00134 | 0.624 |
DOC_MAPK_gen_1 | 178 | 187 | PF00069 | 0.582 |
DOC_MAPK_RevD_3 | 65 | 79 | PF00069 | 0.699 |
DOC_PP1_RVXF_1 | 220 | 227 | PF00149 | 0.592 |
DOC_PP1_RVXF_1 | 330 | 336 | PF00149 | 0.650 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.677 |
DOC_PP2B_LxvP_1 | 203 | 206 | PF13499 | 0.668 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.676 |
DOC_PP2B_LxvP_1 | 351 | 354 | PF13499 | 0.579 |
DOC_PP2B_LxvP_1 | 371 | 374 | PF13499 | 0.374 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.741 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 170 | 180 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 313 | 319 | PF00244 | 0.694 |
LIG_APCC_ABBA_1 | 358 | 363 | PF00400 | 0.659 |
LIG_BIR_III_4 | 132 | 136 | PF00653 | 0.621 |
LIG_CaM_IQ_9 | 185 | 200 | PF13499 | 0.631 |
LIG_deltaCOP1_diTrp_1 | 363 | 369 | PF00928 | 0.671 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.593 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.620 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.644 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.733 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.549 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.672 |
LIG_GBD_Chelix_1 | 338 | 346 | PF00786 | 0.663 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.744 |
LIG_LIR_Gen_1 | 334 | 342 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 343 | 352 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.418 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.741 |
LIG_NRBOX | 183 | 189 | PF00104 | 0.650 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.653 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.621 |
LIG_SH2_STAT3 | 300 | 303 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.560 |
LIG_SUMO_SIM_anti_2 | 183 | 190 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.664 |
LIG_SUMO_SIM_par_1 | 63 | 70 | PF11976 | 0.625 |
LIG_TRFH_1 | 369 | 373 | PF08558 | 0.696 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.610 |
LIG_UBA3_1 | 162 | 171 | PF00899 | 0.646 |
LIG_UBA3_1 | 184 | 193 | PF00899 | 0.675 |
MOD_CDK_SPxxK_3 | 248 | 255 | PF00069 | 0.685 |
MOD_CDK_SPxxK_3 | 304 | 311 | PF00069 | 0.408 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.689 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.619 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.681 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.585 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.736 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.716 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.618 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.772 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.762 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.611 |
MOD_GlcNHglycan | 32 | 38 | PF01048 | 0.602 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.727 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.680 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.535 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.612 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.557 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.497 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.683 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.585 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.636 |
MOD_Plk_2-3 | 319 | 325 | PF00069 | 0.636 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.600 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.677 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.761 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.406 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.745 |
TRG_DiLeu_BaEn_1 | 183 | 188 | PF01217 | 0.636 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 255 | 260 | PF00026 | 0.704 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X7 | Leptomonas seymouri | 34% | 95% |
A4H657 | Leishmania braziliensis | 76% | 100% |
A4HUH7 | Leishmania infantum | 99% | 100% |
E9AN75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QHF0 | Leishmania major | 92% | 100% |