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: 5 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4QCS5
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004175 | endopeptidase activity | 4 | 9 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 9 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 9 |
GO:0008233 | peptidase activity | 3 | 9 |
GO:0008234 | cysteine-type peptidase activity | 4 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 341 | 347 | PF00089 | 0.392 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.453 |
DEG_SPOP_SBC_1 | 122 | 126 | PF00917 | 0.434 |
DOC_ANK_TNKS_1 | 147 | 154 | PF00023 | 0.418 |
DOC_CYCLIN_RxL_1 | 197 | 208 | PF00134 | 0.465 |
DOC_MAPK_gen_1 | 133 | 143 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 297 | 304 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 68 | 77 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 68 | 77 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 198 | 205 | PF00149 | 0.434 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.434 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.463 |
DOC_PP4_FxxP_1 | 320 | 323 | PF00568 | 0.368 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.451 |
LIG_14-3-3_CanoR_1 | 178 | 187 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 34 | 38 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 398 | 404 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 410 | 414 | PF00244 | 0.434 |
LIG_APCC_ABBA_1 | 322 | 327 | PF00400 | 0.399 |
LIG_APCC_ABBAyCdc20_2 | 321 | 327 | PF00400 | 0.395 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.285 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.572 |
LIG_deltaCOP1_diTrp_1 | 305 | 313 | PF00928 | 0.360 |
LIG_EH1_1 | 195 | 203 | PF00400 | 0.465 |
LIG_eIF4E_1 | 210 | 216 | PF01652 | 0.418 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.447 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.510 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.489 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.423 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.478 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.475 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 340 | 349 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 408 | 414 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 79 | 89 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.523 |
LIG_LYPXL_S_1 | 195 | 199 | PF13949 | 0.265 |
LIG_LYPXL_yS_3 | 196 | 199 | PF13949 | 0.465 |
LIG_LYPXL_yS_3 | 379 | 382 | PF13949 | 0.442 |
LIG_MYND_3 | 75 | 79 | PF01753 | 0.434 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.360 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.462 |
LIG_SH2_GRB2like | 60 | 63 | PF00017 | 0.434 |
LIG_SH2_GRB2like | 89 | 92 | PF00017 | 0.465 |
LIG_SH2_PTP2 | 301 | 304 | PF00017 | 0.341 |
LIG_SH2_SRC | 112 | 115 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.470 |
LIG_SH2_STAT3 | 137 | 140 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.477 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.496 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.571 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.516 |
LIG_SUMO_SIM_anti_2 | 119 | 126 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 212 | 217 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 380 | 385 | PF11976 | 0.489 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.338 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.444 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.500 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.576 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.437 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.523 |
MOD_CMANNOS | 239 | 242 | PF00535 | 0.250 |
MOD_CMANNOS | 303 | 306 | PF00535 | 0.350 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.273 |
MOD_GlcNHglycan | 174 | 178 | PF01048 | 0.304 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.461 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.314 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.320 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.552 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.453 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.401 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.435 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.504 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.452 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.457 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.535 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.433 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.462 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.468 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.496 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.445 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.447 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.553 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.392 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.434 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.439 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.465 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.514 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.452 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.504 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.430 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.378 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.554 |
TRG_DiLeu_BaEn_4 | 389 | 395 | PF01217 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NJ61 | Trypanosomatidae | 27% | 73% |
A4HJ23 | Leishmania braziliensis | 30% | 86% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 81% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 71% |
E8NHQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 93% |
E9AIH6 | Leishmania braziliensis | 73% | 76% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 75% |