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: 18 |
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:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 9 |
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:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4QG89
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 2 |
GO:0006605 | protein targeting | 5 | 2 |
GO:0006612 | protein targeting to membrane | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 2 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 2 |
GO:0018345 | protein palmitoylation | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016409 | palmitoyltransferase activity | 5 | 9 |
GO:0016417 | S-acyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 9 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.752 |
CLV_MEL_PAP_1 | 80 | 86 | PF00089 | 0.426 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.434 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.446 |
CLV_Separin_Metazoa | 118 | 122 | PF03568 | 0.671 |
DEG_APCC_DBOX_1 | 249 | 257 | PF00400 | 0.599 |
DEG_APCC_DBOX_1 | 262 | 270 | PF00400 | 0.582 |
DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.495 |
DEG_APCC_DBOX_1 | 500 | 508 | PF00400 | 0.603 |
DEG_Kelch_Keap1_1 | 218 | 223 | PF01344 | 0.677 |
DEG_SIAH_1 | 593 | 601 | PF03145 | 0.687 |
DOC_CKS1_1 | 475 | 480 | PF01111 | 0.589 |
DOC_MAPK_gen_1 | 244 | 255 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 276 | 283 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 248 | 257 | PF00069 | 0.603 |
DOC_MAPK_MEF2A_6 | 497 | 504 | PF00069 | 0.579 |
DOC_MAPK_NFAT4_5 | 497 | 505 | PF00069 | 0.583 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.803 |
DOC_USP7_MATH_2 | 77 | 83 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 128 | 135 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 167 | 171 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 152 | 169 | PF00022 | 0.686 |
LIG_AP2alpha_1 | 492 | 496 | PF02296 | 0.573 |
LIG_APCC_ABBA_1 | 187 | 192 | PF00400 | 0.704 |
LIG_APCC_ABBAyCdc20_2 | 186 | 192 | PF00400 | 0.703 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.658 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.342 |
LIG_EH1_1 | 16 | 24 | PF00400 | 0.573 |
LIG_eIF4E_1 | 17 | 23 | PF01652 | 0.573 |
LIG_eIF4E_1 | 333 | 339 | PF01652 | 0.410 |
LIG_eIF4E_1 | 340 | 346 | PF01652 | 0.340 |
LIG_eIF4E_1 | 41 | 47 | PF01652 | 0.485 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.634 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.677 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.659 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.599 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.725 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.282 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.723 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.677 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.597 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.603 |
LIG_LIR_Apic_2 | 280 | 286 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 142 | 151 | PF02991 | 0.715 |
LIG_LIR_Gen_1 | 32 | 42 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 331 | 341 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 372 | 382 | PF02991 | 0.205 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 32 | 37 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.205 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.739 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.340 |
LIG_NRBOX | 405 | 411 | PF00104 | 0.562 |
LIG_PCNA_PIPBox_1 | 347 | 356 | PF02747 | 0.348 |
LIG_PCNA_yPIPBox_3 | 11 | 20 | PF02747 | 0.616 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.377 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.589 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.302 |
LIG_PTB_Apo_2 | 327 | 334 | PF02174 | 0.495 |
LIG_PTB_Phospho_1 | 327 | 333 | PF10480 | 0.495 |
LIG_REV1ctd_RIR_1 | 360 | 369 | PF16727 | 0.293 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.702 |
LIG_SH2_GRB2like | 328 | 331 | PF00017 | 0.562 |
LIG_SH2_GRB2like | 587 | 590 | PF00017 | 0.672 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.436 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.562 |
LIG_SH2_SRC | 395 | 398 | PF00017 | 0.516 |
LIG_SH2_SRC | 429 | 432 | PF00017 | 0.757 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.162 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.672 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.670 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.551 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.714 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.715 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.381 |
LIG_SUMO_SIM_anti_2 | 254 | 259 | PF11976 | 0.569 |
LIG_SUMO_SIM_anti_2 | 48 | 54 | PF11976 | 0.266 |
LIG_SUMO_SIM_anti_2 | 566 | 573 | PF11976 | 0.660 |
LIG_SUMO_SIM_par_1 | 254 | 259 | PF11976 | 0.569 |
LIG_TRAF2_1 | 172 | 175 | PF00917 | 0.672 |
LIG_TRAF2_1 | 440 | 443 | PF00917 | 0.680 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.638 |
LIG_TYR_ITIM | 338 | 343 | PF00017 | 0.317 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.414 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.614 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.662 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.496 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.632 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.742 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.685 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.589 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.493 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.359 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.628 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.610 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.460 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.656 |
MOD_GlcNHglycan | 223 | 228 | PF01048 | 0.651 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.647 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.399 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.308 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.451 |
MOD_GlcNHglycan | 442 | 447 | PF01048 | 0.617 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.656 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.650 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.707 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.492 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.503 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.566 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.724 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.799 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.407 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.610 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.748 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.679 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.436 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.702 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.348 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.515 |
MOD_N-GLC_1 | 588 | 593 | PF02516 | 0.520 |
MOD_N-GLC_2 | 289 | 291 | PF02516 | 0.348 |
MOD_N-GLC_2 | 309 | 311 | PF02516 | 0.396 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.593 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.624 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.506 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.317 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.390 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.338 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.592 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.310 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.311 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.722 |
MOD_PK_1 | 503 | 509 | PF00069 | 0.486 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.606 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.669 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.561 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.512 |
MOD_PKB_1 | 501 | 509 | PF00069 | 0.483 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.622 |
MOD_Plk_2-3 | 512 | 518 | PF00069 | 0.624 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.381 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.259 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.381 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.357 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.671 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.428 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.625 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.551 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.652 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.544 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.749 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.670 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.504 |
MOD_SUMO_for_1 | 602 | 605 | PF00179 | 0.626 |
TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_2 | 278 | 284 | PF01217 | 0.455 |
TRG_DiLeu_LyEn_5 | 466 | 471 | PF01217 | 0.366 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.162 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.640 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 556 | 559 | PF00400 | 0.643 |
TRG_NES_CRM1_1 | 232 | 246 | PF08389 | 0.566 |
TRG_NLS_MonoExtC_3 | 246 | 251 | PF00514 | 0.561 |
TRG_NLS_MonoExtN_4 | 244 | 251 | PF00514 | 0.567 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7C7 | Leptomonas seymouri | 49% | 96% |
A0A3Q8ICU7 | Leishmania donovani | 92% | 100% |
A4H754 | Leishmania braziliensis | 71% | 99% |
A4HVJ3 | Leishmania infantum | 92% | 100% |
D0A6R2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AP89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5AVF5 | Trypanosoma cruzi | 27% | 100% |