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: 9 |
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 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0008303 | caspase complex | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042765 | GPI-anchor transamidase complex | 3 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905368 | peptidase complex | 3 | 1 |
GO:1905369 | endopeptidase complex | 4 | 1 |
Related structures:
AlphaFold database: A4HKP6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003923 | GPI-anchor transamidase activity | 6 | 1 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008234 | cysteine-type peptidase activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.377 |
DEG_APCC_DBOX_1 | 276 | 284 | PF00400 | 0.392 |
DEG_SCF_FBW7_1 | 70 | 77 | PF00400 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 372 | 378 | PF00134 | 0.450 |
DOC_MAPK_DCC_7 | 224 | 234 | PF00069 | 0.249 |
DOC_MAPK_gen_1 | 354 | 364 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 49 | 56 | PF00069 | 0.403 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.447 |
DOC_PP2B_LxvP_1 | 372 | 375 | PF13499 | 0.382 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.337 |
DOC_PP4_MxPP_1 | 80 | 83 | PF00568 | 0.289 |
DOC_SPAK_OSR1_1 | 399 | 403 | PF12202 | 0.551 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.460 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.615 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 21 | 28 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.340 |
LIG_Actin_WH2_2 | 253 | 270 | PF00022 | 0.314 |
LIG_Actin_WH2_2 | 307 | 324 | PF00022 | 0.407 |
LIG_Actin_WH2_2 | 339 | 356 | PF00022 | 0.432 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.450 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.421 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.300 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.435 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.420 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.432 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.442 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.532 |
LIG_GBD_Chelix_1 | 380 | 388 | PF00786 | 0.399 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 129 | 136 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.521 |
LIG_MYND_1 | 366 | 370 | PF01753 | 0.367 |
LIG_MYND_1 | 74 | 78 | PF01753 | 0.435 |
LIG_MYND_1 | 95 | 99 | PF01753 | 0.412 |
LIG_RPA_C_Fungi | 394 | 406 | PF08784 | 0.333 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.475 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.387 |
LIG_SH2_NCK_1 | 312 | 316 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.443 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.659 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.477 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.476 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.383 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.620 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.468 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 279 | 285 | PF11976 | 0.479 |
LIG_TYR_ITSM | 127 | 134 | PF00017 | 0.493 |
LIG_WRC_WIRS_1 | 290 | 295 | PF05994 | 0.423 |
MOD_CDC14_SPxK_1 | 4 | 7 | PF00782 | 0.661 |
MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.750 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.686 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.703 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.472 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.332 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.490 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.490 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.501 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.660 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.505 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.669 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.411 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.472 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.503 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.354 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.683 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.627 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.529 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.238 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.503 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.667 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.359 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.378 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.460 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.544 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.555 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.326 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.540 |
MOD_PKA_1 | 21 | 27 | PF00069 | 0.566 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.511 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.458 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.390 |
MOD_PKB_1 | 266 | 274 | PF00069 | 0.609 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.537 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.433 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.511 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.696 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.619 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.565 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.742 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.490 |
MOD_SUMO_rev_2 | 417 | 424 | PF00179 | 0.392 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.592 |
TRG_ER_diLys_1 | 437 | 440 | PF00400 | 0.626 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I345 | Leptomonas seymouri | 56% | 100% |
A0A1X0NT15 | Trypanosomatidae | 28% | 100% |
A0A3S5IR84 | Trypanosoma rangeli | 29% | 100% |
A0A3S7X5V4 | Leishmania donovani | 77% | 100% |
A4I877 | Leishmania infantum | 77% | 100% |
D0AAE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9B335 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q519 | Leishmania major | 77% | 100% |
V5AUS2 | Trypanosoma cruzi | 31% | 100% |