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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HQ74
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.788 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.489 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.446 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 181 | 185 | PF00917 | 0.758 |
DOC_CDC14_PxL_1 | 130 | 138 | PF14671 | 0.503 |
DOC_CKS1_1 | 102 | 107 | PF01111 | 0.353 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.657 |
DOC_CYCLIN_RxL_1 | 45 | 53 | PF00134 | 0.521 |
DOC_MAPK_MEF2A_6 | 207 | 215 | PF00069 | 0.530 |
DOC_MIT_MIM_1 | 7 | 17 | PF04212 | 0.432 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.408 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 189 | 194 | PF00244 | 0.774 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 252 | 262 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 38 | 47 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.395 |
LIG_APCC_ABBA_1 | 324 | 329 | PF00400 | 0.634 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.506 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.587 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.611 |
LIG_BRCT_BRCA1_2 | 296 | 302 | PF00533 | 0.464 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.791 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.527 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.513 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.490 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.505 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.686 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.683 |
LIG_GBD_Chelix_1 | 10 | 18 | PF00786 | 0.304 |
LIG_LIR_Gen_1 | 158 | 166 | PF02991 | 0.713 |
LIG_LIR_Gen_1 | 269 | 279 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 318 | 327 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.599 |
LIG_MLH1_MIPbox_1 | 296 | 300 | PF16413 | 0.587 |
LIG_NRBOX | 13 | 19 | PF00104 | 0.310 |
LIG_Pex14_2 | 254 | 258 | PF04695 | 0.515 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.667 |
LIG_REV1ctd_RIR_1 | 296 | 306 | PF16727 | 0.460 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.712 |
LIG_SH2_GRB2like | 272 | 275 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 327 | 331 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.473 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.518 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.712 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.396 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.363 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 167 | 173 | PF11976 | 0.745 |
LIG_SUMO_SIM_anti_2 | 6 | 12 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 99 | 104 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 76 | 83 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 96 | 104 | PF11976 | 0.247 |
LIG_WW_3 | 138 | 142 | PF00397 | 0.498 |
MOD_CDK_SPxK_1 | 135 | 141 | PF00069 | 0.625 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.718 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.736 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.406 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.566 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.542 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.783 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.672 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.502 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.754 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.529 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.495 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.528 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.647 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.596 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.687 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.534 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.600 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.599 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.620 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.632 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.580 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.775 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.669 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.514 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.448 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.683 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.559 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.575 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.748 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.460 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.583 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.392 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.747 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.442 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.559 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.388 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.549 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.622 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.532 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.522 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.746 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.403 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.350 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.616 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.475 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.509 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.522 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.591 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.683 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 131 | 136 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.714 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 48 | 53 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P9D5 | Leptomonas seymouri | 70% | 97% |
A0A1X0P057 | Trypanosomatidae | 31% | 100% |
A0A3R7RKF3 | Trypanosoma rangeli | 36% | 100% |
A0A3S7XBW0 | Leishmania donovani | 81% | 98% |
A4IDX2 | Leishmania infantum | 82% | 98% |
D0A445 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ATZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 98% |
Q4Q0K3 | Leishmania major | 81% | 100% |
V5B3M7 | Trypanosoma cruzi | 35% | 100% |