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: A0A3Q8IE12
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005543 | phospholipid binding | 3 | 1 |
GO:0008289 | lipid binding | 2 | 1 |
GO:0032182 | ubiquitin-like protein binding | 3 | 1 |
GO:0035091 | phosphatidylinositol binding | 4 | 1 |
GO:0043130 | ubiquitin binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.748 |
CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 42 | 46 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.432 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.754 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.521 |
DEG_SCF_FBW7_1 | 241 | 248 | PF00400 | 0.738 |
DEG_SPOP_SBC_1 | 249 | 253 | PF00917 | 0.761 |
DEG_SPOP_SBC_1 | 339 | 343 | PF00917 | 0.628 |
DOC_CYCLIN_RxL_1 | 193 | 202 | PF00134 | 0.754 |
DOC_MAPK_DCC_7 | 265 | 275 | PF00069 | 0.714 |
DOC_MAPK_gen_1 | 114 | 123 | PF00069 | 0.564 |
DOC_MAPK_HePTP_8 | 263 | 275 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 266 | 275 | PF00069 | 0.714 |
DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.669 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.590 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.723 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.773 |
LIG_14-3-3_CanoR_1 | 120 | 124 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 138 | 146 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 149 | 155 | PF00244 | 0.560 |
LIG_APCC_ABBA_1 | 55 | 60 | PF00400 | 0.529 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.456 |
LIG_Clathr_ClatBox_1 | 71 | 75 | PF01394 | 0.537 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.437 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.705 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.592 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.482 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.369 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.478 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.665 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.558 |
LIG_LIR_Apic_2 | 322 | 328 | PF02991 | 0.616 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 125 | 131 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 365 | 376 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 32 | 36 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.617 |
LIG_PTB_Apo_2 | 79 | 86 | PF02174 | 0.561 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.552 |
LIG_SH2_GRB2like | 214 | 217 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 368 | 372 | PF00017 | 0.568 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.581 |
LIG_SH2_SRC | 214 | 217 | PF00017 | 0.591 |
LIG_SH2_SRC | 325 | 328 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.552 |
LIG_SH2_STAT3 | 93 | 96 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.471 |
LIG_SH3_1 | 265 | 271 | PF00018 | 0.677 |
LIG_SH3_1 | 28 | 34 | PF00018 | 0.557 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.598 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.562 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.772 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.557 |
LIG_SUMO_SIM_par_1 | 70 | 75 | PF11976 | 0.434 |
LIG_TYR_ITIM | 124 | 129 | PF00017 | 0.565 |
LIG_UBA3_1 | 175 | 181 | PF00899 | 0.600 |
LIG_UBA3_1 | 99 | 105 | PF00899 | 0.496 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.581 |
LIG_WW_2 | 271 | 274 | PF00397 | 0.684 |
MOD_CDK_SPK_2 | 176 | 181 | PF00069 | 0.606 |
MOD_CDK_SPK_2 | 241 | 246 | PF00069 | 0.717 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.714 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.727 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.745 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.709 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.651 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.551 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.506 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.691 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.725 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.732 |
MOD_Cter_Amidation | 263 | 266 | PF01082 | 0.692 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.508 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.753 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.720 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.284 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.734 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.608 |
MOD_GlcNHglycan | 346 | 350 | PF01048 | 0.664 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.452 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.535 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.608 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.572 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.712 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.723 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.650 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.740 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.642 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.569 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.734 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.570 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.416 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.373 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.674 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.686 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.731 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.478 |
MOD_NEK2_2 | 225 | 230 | PF00069 | 0.624 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.426 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.720 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.551 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.293 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.525 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.440 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.607 |
MOD_Plk_2-3 | 39 | 45 | PF00069 | 0.556 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.561 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.519 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.561 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.716 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.713 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.564 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.772 |
TRG_DiLeu_BaEn_2 | 31 | 37 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.707 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.421 |
TRG_NES_CRM1_1 | 94 | 108 | PF08389 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 156 | 161 | PF00026 | 0.613 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JFL9 | Bodo saltans | 29% | 92% |
A4HHW6 | Leishmania braziliensis | 72% | 100% |
A4I516 | Leishmania infantum | 100% | 100% |
E9B0E6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q7T7 | Leishmania major | 88% | 100% |