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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 9 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0070765 | gamma-secretase complex | 3 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0098797 | plasma membrane protein complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:1902494 | catalytic complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QGS9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0016485 | protein processing | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0043085 | positive regulation of catalytic activity | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044093 | positive regulation of molecular function | 3 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0050790 | regulation of catalytic activity | 3 | 9 |
GO:0051604 | protein maturation | 4 | 9 |
GO:0065007 | biological regulation | 1 | 9 |
GO:0065009 | regulation of molecular function | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.651 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.651 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.664 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.559 |
DEG_SPOP_SBC_1 | 150 | 154 | PF00917 | 0.452 |
DEG_SPOP_SBC_1 | 231 | 235 | PF00917 | 0.688 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.647 |
DOC_MAPK_DCC_7 | 105 | 115 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 105 | 113 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 82 | 90 | PF00069 | 0.598 |
DOC_PP1_RVXF_1 | 92 | 98 | PF00149 | 0.627 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.438 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.453 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.740 |
LIG_14-3-3_CanoR_1 | 149 | 156 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 307 | 315 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 339 | 349 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 415 | 422 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.668 |
LIG_Actin_WH2_2 | 41 | 59 | PF00022 | 0.490 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.408 |
LIG_Clathr_ClatBox_1 | 262 | 266 | PF01394 | 0.732 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.531 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.802 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.705 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.334 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.719 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.457 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.561 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.706 |
LIG_LIR_Gen_1 | 2 | 8 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 450 | 458 | PF02991 | 0.698 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 450 | 454 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.454 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.480 |
LIG_PCNA_yPIPBox_3 | 416 | 430 | PF02747 | 0.303 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.396 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.310 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.638 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.663 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.404 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.570 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.691 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.734 |
LIG_SUMO_SIM_anti_2 | 261 | 267 | PF11976 | 0.668 |
LIG_SUMO_SIM_anti_2 | 431 | 437 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 261 | 267 | PF11976 | 0.730 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.596 |
LIG_SUMO_SIM_par_1 | 4 | 10 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 440 | 445 | PF11976 | 0.493 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.797 |
LIG_TRFH_1 | 108 | 112 | PF08558 | 0.596 |
LIG_TRFH_1 | 390 | 394 | PF08558 | 0.438 |
LIG_TYR_ITIM | 308 | 313 | PF00017 | 0.638 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.546 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.334 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.736 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.756 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.733 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.474 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.747 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.784 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.771 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.727 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.382 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.566 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.701 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.594 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.596 |
MOD_GlcNHglycan | 316 | 320 | PF01048 | 0.517 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.607 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.464 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.493 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.627 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.532 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.778 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.790 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.760 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.793 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.518 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.621 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.593 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.359 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.435 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.386 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.625 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.325 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.437 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.460 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.301 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.769 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.321 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.586 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.402 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.821 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.781 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.702 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.627 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.532 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.442 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.761 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.475 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.795 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.412 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.601 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.379 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.394 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.423 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.579 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.396 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.736 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.746 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.688 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.779 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY04 | Leptomonas seymouri | 42% | 96% |
A0A3S7WRT9 | Leishmania donovani | 87% | 100% |
A0A422NUD7 | Trypanosoma rangeli | 27% | 100% |
A4H6T0 | Leishmania braziliensis | 66% | 100% |
A4HV58 | Leishmania infantum | 88% | 68% |
E9ANU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
V5BDA4 | Trypanosoma cruzi | 24% | 100% |