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: E9AIX0
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.729 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.502 |
CLV_PCSK_FUR_1 | 182 | 186 | PF00082 | 0.525 |
CLV_PCSK_FUR_1 | 190 | 194 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.430 |
CLV_PCSK_PC7_1 | 136 | 142 | PF00082 | 0.541 |
CLV_PCSK_PC7_1 | 185 | 191 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.496 |
DOC_MAPK_gen_1 | 306 | 314 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.337 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.665 |
DOC_PP4_FxxP_1 | 292 | 295 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.430 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.583 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 34 | 40 | PF00244 | 0.564 |
LIG_Actin_WH2_2 | 250 | 265 | PF00022 | 0.688 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.641 |
LIG_deltaCOP1_diTrp_1 | 228 | 232 | PF00928 | 0.668 |
LIG_eIF4E_1 | 240 | 246 | PF01652 | 0.523 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.354 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 290 | 295 | PF02991 | 0.501 |
LIG_LIR_Apic_2 | 298 | 302 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 52 | 60 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.482 |
LIG_PTB_Apo_2 | 302 | 309 | PF02174 | 0.359 |
LIG_PTB_Phospho_1 | 302 | 308 | PF10480 | 0.356 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.430 |
LIG_SH2_NCK_1 | 362 | 366 | PF00017 | 0.249 |
LIG_SH2_PTP2 | 53 | 56 | PF00017 | 0.514 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.249 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.514 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.376 |
LIG_SUMO_SIM_par_1 | 6 | 12 | PF11976 | 0.511 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.547 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.620 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.600 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.574 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.575 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.563 |
LIG_TRFH_1 | 373 | 377 | PF08558 | 0.614 |
LIG_TYR_ITIM | 51 | 56 | PF00017 | 0.521 |
LIG_UBA3_1 | 35 | 40 | PF00899 | 0.508 |
LIG_WW_3 | 294 | 298 | PF00397 | 0.380 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.751 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.510 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.523 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.574 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.562 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.249 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.430 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.591 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.632 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.744 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.541 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.499 |
MOD_NEK2_2 | 19 | 24 | PF00069 | 0.724 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.364 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.407 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.493 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.430 |
MOD_PKB_1 | 124 | 132 | PF00069 | 0.453 |
MOD_Plk_2-3 | 52 | 58 | PF00069 | 0.474 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.510 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.500 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.694 |
MOD_SUMO_rev_2 | 199 | 206 | PF00179 | 0.459 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_4 | 202 | 208 | PF01217 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 373 | 376 | PF00400 | 0.526 |
TRG_NES_CRM1_1 | 46 | 58 | PF08389 | 0.467 |
TRG_NLS_MonoCore_2 | 188 | 193 | PF00514 | 0.542 |
TRG_NLS_MonoExtC_3 | 188 | 193 | PF00514 | 0.542 |
TRG_NLS_MonoExtC_3 | 216 | 221 | PF00514 | 0.432 |
TRG_NLS_MonoExtN_4 | 188 | 193 | PF00514 | 0.546 |
TRG_NLS_MonoExtN_4 | 217 | 222 | PF00514 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 141 | 146 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 354 | 358 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 37 | 42 | PF00026 | 0.667 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3I7 | Leptomonas seymouri | 78% | 95% |
A0A0S4JE94 | Bodo saltans | 54% | 100% |
A0A3S5H806 | Leishmania donovani | 88% | 100% |
A4IBW6 | Leishmania infantum | 88% | 100% |
E9AFQ3 | Leishmania major | 87% | 100% |
E9B6V6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |