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: A4HSS7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.570 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.568 |
DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.459 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 239 | 245 | PF00134 | 0.543 |
DOC_MAPK_gen_1 | 196 | 204 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 331 | 338 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 395 | 401 | PF00069 | 0.707 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.574 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.670 |
DOC_PP4_FxxP_1 | 107 | 110 | PF00568 | 0.649 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.548 |
DOC_USP7_UBL2_3 | 327 | 331 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 284 | 293 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 407 | 417 | PF00244 | 0.718 |
LIG_Actin_WH2_2 | 139 | 156 | PF00022 | 0.531 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.591 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.570 |
LIG_Clathr_ClatBox_1 | 436 | 440 | PF01394 | 0.682 |
LIG_deltaCOP1_diTrp_1 | 212 | 219 | PF00928 | 0.536 |
LIG_DLG_GKlike_1 | 260 | 267 | PF00625 | 0.485 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.482 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.662 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.575 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.739 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.643 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.691 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.602 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.683 |
LIG_GBD_Chelix_1 | 88 | 96 | PF00786 | 0.647 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 263 | 272 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 367 | 374 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.627 |
LIG_NRBOX | 222 | 228 | PF00104 | 0.493 |
LIG_PDZ_Class_3 | 446 | 451 | PF00595 | 0.678 |
LIG_SH2_SRC | 314 | 317 | PF00017 | 0.600 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.615 |
LIG_SH3_4 | 327 | 334 | PF00018 | 0.521 |
LIG_Sin3_1 | 223 | 233 | PF02671 | 0.462 |
LIG_SUMO_SIM_par_1 | 251 | 258 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 269 | 276 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 431 | 440 | PF11976 | 0.696 |
LIG_TYR_ITIM | 262 | 267 | PF00017 | 0.403 |
LIG_UBA3_1 | 92 | 101 | PF00899 | 0.535 |
LIG_WRC_WIRS_1 | 174 | 179 | PF05994 | 0.499 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.402 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.577 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.456 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.602 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.669 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.651 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.584 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.656 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.616 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.492 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.554 |
MOD_Cter_Amidation | 258 | 261 | PF01082 | 0.533 |
MOD_Cter_Amidation | 331 | 334 | PF01082 | 0.732 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.588 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.489 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.455 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.511 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.704 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.515 |
MOD_GlcNHglycan | 323 | 327 | PF01048 | 0.409 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.567 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.653 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.726 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.480 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.605 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.382 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.611 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.730 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.468 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.493 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.417 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.298 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.454 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.362 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.706 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.636 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.555 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.636 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.447 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.413 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.435 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.564 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.675 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.567 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.521 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.568 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.512 |
MOD_OFUCOSY | 105 | 112 | PF10250 | 0.722 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.740 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.424 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.486 |
MOD_PKA_1 | 403 | 409 | PF00069 | 0.671 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.468 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.437 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.598 |
MOD_PKB_1 | 405 | 413 | PF00069 | 0.650 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.492 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.462 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.600 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.428 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.535 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.551 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.537 |
MOD_SUMO_for_1 | 309 | 312 | PF00179 | 0.609 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.613 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.655 |
TRG_NLS_MonoExtC_3 | 402 | 407 | PF00514 | 0.650 |
TRG_NLS_MonoExtN_4 | 403 | 408 | PF00514 | 0.717 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZQ7 | Leptomonas seymouri | 46% | 100% |
A0A1X0NL47 | Trypanosomatidae | 33% | 98% |
A0A3S5H5P7 | Leishmania donovani | 99% | 100% |
A0A3S5IR10 | Trypanosoma rangeli | 30% | 97% |
A4H4K1 | Leishmania braziliensis | 78% | 100% |
C9ZTC6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 98% |
E9AKR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QJ43 | Leishmania major | 95% | 100% |
V5BA95 | Trypanosoma cruzi | 32% | 98% |