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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9ANN7
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.585 |
CLV_PCSK_FUR_1 | 117 | 121 | PF00082 | 0.314 |
CLV_PCSK_FUR_1 | 338 | 342 | PF00082 | 0.776 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.498 |
CLV_PCSK_PC7_1 | 83 | 89 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.664 |
CLV_Separin_Metazoa | 64 | 68 | PF03568 | 0.453 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.499 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 22 | 30 | PF00134 | 0.611 |
DOC_MAPK_gen_1 | 21 | 28 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.609 |
DOC_MAPK_NFAT4_5 | 21 | 29 | PF00069 | 0.572 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.424 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 132 | 136 | PF12436 | 0.594 |
DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.687 |
DOC_USP7_UBL2_3 | 311 | 315 | PF12436 | 0.670 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 340 | 349 | PF00244 | 0.504 |
LIG_Actin_WH2_2 | 105 | 121 | PF00022 | 0.361 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.624 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.512 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.595 |
LIG_LIR_Gen_1 | 154 | 161 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 254 | 265 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.502 |
LIG_NRP_CendR_1 | 374 | 377 | PF00754 | 0.632 |
LIG_SH2_PTP2 | 257 | 260 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.481 |
LIG_SH3_1 | 150 | 156 | PF00018 | 0.609 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.706 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.563 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.630 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.551 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.527 |
LIG_SH3_4 | 311 | 318 | PF00018 | 0.672 |
LIG_SUMO_SIM_anti_2 | 219 | 226 | PF11976 | 0.612 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.539 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.653 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.475 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.495 |
MOD_CDK_SPK_2 | 333 | 338 | PF00069 | 0.719 |
MOD_CDK_SPK_2 | 345 | 350 | PF00069 | 0.498 |
MOD_CDK_SPK_2 | 66 | 71 | PF00069 | 0.475 |
MOD_CDK_SPxxK_3 | 333 | 340 | PF00069 | 0.604 |
MOD_CDK_SPxxK_3 | 345 | 352 | PF00069 | 0.500 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.620 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.516 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.657 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.679 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.609 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.512 |
MOD_DYRK1A_RPxSP_1 | 333 | 337 | PF00069 | 0.603 |
MOD_GlcNHglycan | 163 | 167 | PF01048 | 0.488 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.491 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.527 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.462 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.526 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.578 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.566 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.459 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.702 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.644 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.633 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.466 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.796 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.729 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.541 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.625 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.582 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.602 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.469 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.462 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.397 |
MOD_PK_1 | 272 | 278 | PF00069 | 0.603 |
MOD_PKA_1 | 278 | 284 | PF00069 | 0.530 |
MOD_PKA_1 | 340 | 346 | PF00069 | 0.741 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.556 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.519 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.559 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.741 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.637 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.613 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.433 |
MOD_PKB_1 | 318 | 326 | PF00069 | 0.573 |
MOD_PKB_1 | 338 | 346 | PF00069 | 0.633 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.554 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.619 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.488 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.632 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.364 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.690 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.736 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.602 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.511 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.494 |
MOD_SUMO_for_1 | 161 | 164 | PF00179 | 0.638 |
MOD_SUMO_for_1 | 183 | 186 | PF00179 | 0.676 |
MOD_SUMO_rev_2 | 171 | 177 | PF00179 | 0.704 |
MOD_SUMO_rev_2 | 178 | 185 | PF00179 | 0.704 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_2 | 146 | 152 | PF01217 | 0.624 |
TRG_DiLeu_BaEn_4 | 123 | 129 | PF01217 | 0.377 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.581 |
TRG_NLS_MonoExtC_3 | 307 | 312 | PF00514 | 0.661 |
TRG_NLS_MonoExtN_4 | 306 | 312 | PF00514 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7D2 | Leptomonas seymouri | 53% | 84% |
A0A1X0NWL9 | Trypanosomatidae | 32% | 80% |
A0A3R7LWS6 | Trypanosoma rangeli | 34% | 81% |
A0A3S7WRS1 | Leishmania donovani | 92% | 100% |
A4H6L9 | Leishmania braziliensis | 84% | 100% |
A4HV02 | Leishmania infantum | 93% | 100% |
Q4QGY6 | Leishmania major | 92% | 100% |
V5DT45 | Trypanosoma cruzi | 35% | 81% |