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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A0A3S7WUI4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.598 |
CLV_MEL_PAP_1 | 198 | 204 | PF00089 | 0.405 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.395 |
CLV_PCSK_FUR_1 | 365 | 369 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.406 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.641 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.406 |
DOC_CYCLIN_yCln2_LP_2 | 232 | 238 | PF00134 | 0.427 |
DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.442 |
DOC_CYCLIN_yCln2_LP_2 | 47 | 53 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 213 | 223 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 333 | 343 | PF00069 | 0.610 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 411 | 418 | PF00069 | 0.633 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.611 |
DOC_PP1_RVXF_1 | 302 | 308 | PF00149 | 0.610 |
DOC_PP1_RVXF_1 | 82 | 89 | PF00149 | 0.566 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.389 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.434 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.380 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.360 |
DOC_PP4_FxxP_1 | 280 | 283 | PF00568 | 0.648 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 356 | 360 | PF12436 | 0.681 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 368 | 374 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 387 | 392 | PF00244 | 0.783 |
LIG_Actin_WH2_2 | 252 | 268 | PF00022 | 0.420 |
LIG_APCC_ABBA_1 | 341 | 346 | PF00400 | 0.648 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.427 |
LIG_Clathr_ClatBox_1 | 176 | 180 | PF01394 | 0.427 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.579 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.403 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.372 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.679 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.395 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.474 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.684 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.627 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.694 |
LIG_LIR_Gen_1 | 190 | 198 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.539 |
LIG_MYND_1 | 250 | 254 | PF01753 | 0.336 |
LIG_PCNA_yPIPBox_3 | 201 | 212 | PF02747 | 0.566 |
LIG_RPA_C_Insects | 86 | 101 | PF08784 | 0.471 |
LIG_SH2_SRC | 76 | 79 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 328 | 332 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 285 | 288 | PF00017 | 0.584 |
LIG_SH2_STAT3 | 54 | 57 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.536 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.587 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 151 | 156 | PF11976 | 0.485 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.733 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.589 |
LIG_WRC_WIRS_1 | 137 | 142 | PF05994 | 0.486 |
MOD_CDK_SPxxK_3 | 2 | 9 | PF00069 | 0.550 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.516 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.285 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.624 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.390 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.346 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.567 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.705 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.666 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.730 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.665 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.420 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.628 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.436 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.425 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.783 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.181 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.626 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.360 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.334 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.601 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.753 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.636 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.467 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.550 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.439 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.497 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.596 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.321 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.507 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.606 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.384 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.720 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.380 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.434 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.527 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.660 |
MOD_PKA_1 | 387 | 393 | PF00069 | 0.575 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.678 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.380 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.324 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.393 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.317 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.333 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.417 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.513 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.553 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.514 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 426 | 429 | PF00400 | 0.554 |
TRG_NLS_MonoCore_2 | 357 | 362 | PF00514 | 0.608 |
TRG_NLS_MonoExtN_4 | 356 | 363 | PF00514 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 196 | 200 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 324 | 329 | PF00026 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3N4 | Leptomonas seymouri | 61% | 94% |
A0A0S4KHH7 | Bodo saltans | 36% | 90% |
A0A1X0NTB3 | Trypanosomatidae | 48% | 100% |
A4H918 | Leishmania braziliensis | 84% | 100% |
A4HXF0 | Leishmania infantum | 100% | 100% |
C9ZP21 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AR45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QEB8 | Leishmania major | 98% | 100% |
V5BFE7 | Trypanosoma cruzi | 46% | 100% |