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: A4H6T0
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_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.646 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.476 |
DEG_APCC_DBOX_1 | 105 | 113 | PF00400 | 0.272 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.521 |
DEG_SPOP_SBC_1 | 150 | 154 | PF00917 | 0.636 |
DOC_CDC14_PxL_1 | 388 | 396 | PF14671 | 0.235 |
DOC_CKS1_1 | 346 | 351 | PF01111 | 0.654 |
DOC_CYCLIN_yCln2_LP_2 | 25 | 31 | PF00134 | 0.377 |
DOC_MAPK_DCC_7 | 104 | 114 | PF00069 | 0.255 |
DOC_MAPK_gen_1 | 104 | 112 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 104 | 112 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 81 | 89 | PF00069 | 0.337 |
DOC_PP1_RVXF_1 | 91 | 97 | PF00149 | 0.343 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.377 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.364 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.293 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.725 |
LIG_14-3-3_CanoR_1 | 174 | 184 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 338 | 343 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 405 | 409 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 414 | 423 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.658 |
LIG_Actin_WH2_2 | 40 | 58 | PF00022 | 0.377 |
LIG_AP_GAE_1 | 265 | 271 | PF02883 | 0.620 |
LIG_Clathr_ClatBox_1 | 261 | 265 | PF01394 | 0.679 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.230 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.489 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.729 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.420 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.680 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.364 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.454 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.245 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.677 |
LIG_GBD_Chelix_1 | 383 | 391 | PF00786 | 0.261 |
LIG_IRF3_LxIS_1 | 28 | 34 | PF10401 | 0.220 |
LIG_IRF3_LxIS_1 | 5 | 10 | PF10401 | 0.235 |
LIG_LIR_Gen_1 | 38 | 47 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 448 | 454 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 448 | 453 | PF02991 | 0.634 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.506 |
LIG_SH2_CRK | 450 | 454 | PF00017 | 0.660 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 200 | 204 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.655 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.406 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.652 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.277 |
LIG_SUMO_SIM_anti_2 | 430 | 436 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 260 | 267 | PF11976 | 0.676 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 427 | 433 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 43 | 48 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 439 | 444 | PF11976 | 0.425 |
LIG_SxIP_EBH_1 | 402 | 415 | PF03271 | 0.375 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.624 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.737 |
LIG_TRFH_1 | 107 | 111 | PF08558 | 0.322 |
LIG_TRFH_1 | 389 | 393 | PF08558 | 0.308 |
LIG_TRFH_1 | 450 | 454 | PF08558 | 0.595 |
LIG_WRC_WIRS_1 | 36 | 41 | PF05994 | 0.320 |
MOD_CDK_SPxxK_3 | 327 | 334 | PF00069 | 0.647 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.674 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.601 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.639 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.642 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.663 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.753 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.744 |
MOD_CMANNOS | 436 | 439 | PF00535 | 0.228 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.296 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.443 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.393 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.498 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.485 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.564 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.549 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.638 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.601 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.634 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.293 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.681 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.723 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.636 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.325 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.839 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.639 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.420 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.435 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.492 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.558 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.548 |
MOD_N-GLC_2 | 417 | 419 | PF02516 | 0.420 |
MOD_N-GLC_2 | 86 | 88 | PF02516 | 0.466 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.470 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.385 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.196 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.581 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.521 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.589 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.304 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.312 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.528 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.249 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.707 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.817 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.451 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.385 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.496 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.468 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.706 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.352 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.308 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.252 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.553 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.349 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.574 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.389 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.308 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.621 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.724 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.645 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.722 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.644 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.390 |
TRG_NES_CRM1_1 | 252 | 267 | PF08389 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 141 | 145 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY04 | Leptomonas seymouri | 41% | 96% |
A0A3S7WRT9 | Leishmania donovani | 66% | 100% |
A4HV58 | Leishmania infantum | 66% | 68% |
E9ANU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q4QGS9 | Leishmania major | 66% | 100% |