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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0070765 | gamma-secretase complex | 3 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098797 | plasma membrane protein complex | 3 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9ANU1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0016485 | protein processing | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0043085 | positive regulation of catalytic activity | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044093 | positive regulation of molecular function | 3 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0050790 | regulation of catalytic activity | 3 | 7 |
GO:0051604 | protein maturation | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.412 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.266 |
DEG_SPOP_SBC_1 | 231 | 235 | PF00917 | 0.655 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.358 |
DOC_MAPK_DCC_7 | 105 | 115 | PF00069 | 0.250 |
DOC_MAPK_gen_1 | 105 | 113 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.334 |
DOC_PP1_RVXF_1 | 92 | 98 | PF00149 | 0.333 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.358 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.267 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 287 | 297 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 307 | 315 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 435 | 441 | PF00244 | 0.628 |
LIG_Actin_WH2_2 | 41 | 59 | PF00022 | 0.358 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.554 |
LIG_Clathr_ClatBox_1 | 262 | 266 | PF01394 | 0.673 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.808 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.483 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.297 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.643 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.460 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.650 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.632 |
LIG_GBD_Chelix_1 | 373 | 381 | PF00786 | 0.253 |
LIG_Integrin_isoDGR_2 | 147 | 149 | PF01839 | 0.382 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 439 | 447 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 439 | 443 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.311 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.591 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.540 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.477 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.450 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.616 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.572 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.371 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.270 |
LIG_Sin3_3 | 371 | 378 | PF02671 | 0.250 |
LIG_SUMO_SIM_anti_2 | 260 | 268 | PF11976 | 0.640 |
LIG_SUMO_SIM_anti_2 | 420 | 426 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 260 | 268 | PF11976 | 0.671 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 429 | 434 | PF11976 | 0.420 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.574 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.731 |
LIG_TRFH_1 | 108 | 112 | PF08558 | 0.308 |
LIG_TRFH_1 | 379 | 383 | PF08558 | 0.299 |
LIG_WRC_WIRS_1 | 37 | 42 | PF05994 | 0.270 |
MOD_CDK_SPxxK_3 | 398 | 405 | PF00069 | 0.371 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.762 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.474 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.786 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.455 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.649 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.683 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.693 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.353 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.489 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.472 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.629 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.516 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.405 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.638 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.676 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.693 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.420 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.677 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.597 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.321 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.359 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.536 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.377 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.556 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.324 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.385 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.718 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.665 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.655 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.568 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.572 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.845 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.758 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.340 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.299 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.568 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.379 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.567 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.299 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.398 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.608 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 247 | 252 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY04 | Leptomonas seymouri | 42% | 94% |
A0A3S7WRT9 | Leishmania donovani | 83% | 99% |
A4H6T0 | Leishmania braziliensis | 66% | 100% |
A4HV58 | Leishmania infantum | 83% | 67% |
Q4QGS9 | Leishmania major | 82% | 100% |