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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q9G0
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 12 |
GO:0005996 | monosaccharide metabolic process | 3 | 12 |
GO:0006000 | fructose metabolic process | 5 | 12 |
GO:0006003 | fructose 2,6-bisphosphate metabolic process | 4 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019318 | hexose metabolic process | 4 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003873 | 6-phosphofructo-2-kinase activity | 6 | 12 |
GO:0004331 | fructose-2,6-bisphosphate 2-phosphatase activity | 8 | 7 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008443 | phosphofructokinase activity | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019200 | carbohydrate kinase activity | 5 | 12 |
GO:0019203 | carbohydrate phosphatase activity | 6 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0050308 | sugar-phosphatase activity | 7 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 653 | 657 | PF00656 | 0.451 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.121 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.305 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.170 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.420 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.373 |
DOC_CYCLIN_RxL_1 | 458 | 471 | PF00134 | 0.482 |
DOC_CYCLIN_RxL_1 | 518 | 532 | PF00134 | 0.440 |
DOC_CYCLIN_yClb1_LxF_4 | 416 | 421 | PF00134 | 0.424 |
DOC_MAPK_DCC_7 | 29 | 38 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 29 | 38 | PF00069 | 0.692 |
DOC_MAPK_MEF2A_6 | 135 | 143 | PF00069 | 0.451 |
DOC_PP1_RVXF_1 | 249 | 255 | PF00149 | 0.218 |
DOC_PP1_RVXF_1 | 32 | 39 | PF00149 | 0.672 |
DOC_PP1_RVXF_1 | 335 | 341 | PF00149 | 0.304 |
DOC_PP1_RVXF_1 | 416 | 422 | PF00149 | 0.424 |
DOC_PP1_RVXF_1 | 522 | 529 | PF00149 | 0.451 |
DOC_PP2B_PxIxI_1 | 395 | 401 | PF00149 | 0.373 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.218 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.667 |
DOC_USP7_UBL2_3 | 30 | 34 | PF12436 | 0.681 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.402 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 454 | 462 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 489 | 495 | PF00244 | 0.364 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.724 |
LIG_BIR_III_4 | 102 | 106 | PF00653 | 0.508 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.424 |
LIG_Dynein_DLC8_1 | 487 | 493 | PF01221 | 0.438 |
LIG_eIF4E_1 | 121 | 127 | PF01652 | 0.424 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.373 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.467 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.326 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.308 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.329 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.486 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.279 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.332 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.676 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.543 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.369 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.426 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.353 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.345 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.339 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.528 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.667 |
LIG_Integrin_isoDGR_2 | 133 | 135 | PF01839 | 0.451 |
LIG_LIR_Apic_2 | 189 | 195 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 208 | 217 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 37 | 44 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 371 | 382 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 394 | 402 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 440 | 449 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 628 | 639 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 440 | 444 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 628 | 634 | PF02991 | 0.409 |
LIG_MLH1_MIPbox_1 | 175 | 179 | PF16413 | 0.413 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.320 |
LIG_SH2_PTP2 | 397 | 400 | PF00017 | 0.320 |
LIG_SH2_PTP2 | 441 | 444 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.304 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.601 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.220 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.460 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.389 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.670 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 137 | 144 | PF11976 | 0.373 |
LIG_SUMO_SIM_anti_2 | 219 | 225 | PF11976 | 0.320 |
LIG_SUMO_SIM_anti_2 | 304 | 311 | PF11976 | 0.323 |
LIG_SUMO_SIM_anti_2 | 440 | 446 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 476 | 485 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 139 | 144 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 158 | 165 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 591 | 599 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 88 | 93 | PF11976 | 0.435 |
LIG_TYR_ITAM | 371 | 387 | PF00017 | 0.339 |
LIG_UBA3_1 | 223 | 232 | PF00899 | 0.304 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.373 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.624 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.518 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.388 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.389 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.424 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.415 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.424 |
MOD_CK2_1 | 658 | 664 | PF00069 | 0.517 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.748 |
MOD_GlcNHglycan | 144 | 148 | PF01048 | 0.393 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.370 |
MOD_GlcNHglycan | 208 | 212 | PF01048 | 0.657 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.376 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.455 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.218 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.667 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.437 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.451 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.320 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.339 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.511 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.409 |
MOD_N-GLC_1 | 424 | 429 | PF02516 | 0.389 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.675 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.328 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.316 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.379 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.304 |
MOD_NEK2_2 | 490 | 495 | PF00069 | 0.389 |
MOD_NEK2_2 | 498 | 503 | PF00069 | 0.441 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.397 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.451 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.424 |
MOD_PKA_1 | 488 | 494 | PF00069 | 0.470 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.373 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.342 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.364 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.424 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.362 |
MOD_PKB_1 | 458 | 466 | PF00069 | 0.506 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.413 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.580 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.339 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.424 |
MOD_Plk_1 | 498 | 504 | PF00069 | 0.445 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.448 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.380 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.308 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.317 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.421 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.451 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.333 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.310 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.618 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.389 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.373 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.393 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.402 |
MOD_SUMO_rev_2 | 56 | 66 | PF00179 | 0.649 |
TRG_DiLeu_BaEn_1 | 440 | 445 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 328 | 333 | PF01217 | 0.373 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.424 |
TRG_NES_CRM1_1 | 80 | 93 | PF08389 | 0.474 |
TRG_NLS_MonoCore_2 | 28 | 33 | PF00514 | 0.704 |
TRG_NLS_MonoExtC_3 | 29 | 34 | PF00514 | 0.708 |
TRG_NLS_MonoExtN_4 | 29 | 34 | PF00514 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 464 | 468 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXF4 | Leptomonas seymouri | 73% | 98% |
A0A0S4IN06 | Bodo saltans | 44% | 90% |
A0A0S4KH03 | Bodo saltans | 24% | 100% |
A0A1X0NU02 | Trypanosomatidae | 53% | 100% |
A0A3R7MQ36 | Trypanosoma rangeli | 55% | 100% |
A0A3S7WZP0 | Leishmania donovani | 96% | 100% |
A4HEN8 | Leishmania braziliensis | 85% | 100% |
A4I1W7 | Leishmania infantum | 96% | 100% |
C9ZS53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
C9ZUM0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 21% | 95% |
E9AY13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O35552 | Rattus norvegicus | 27% | 100% |
P07953 | Rattus norvegicus | 29% | 100% |
P16118 | Homo sapiens | 28% | 100% |
P25114 | Rattus norvegicus | 28% | 100% |
P40433 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 81% |
P49872 | Bos taurus | 29% | 100% |
P70265 | Mus musculus | 27% | 100% |
Q16875 | Homo sapiens | 27% | 100% |
Q16877 | Homo sapiens | 28% | 100% |
Q21122 | Caenorhabditis elegans | 29% | 100% |
Q28901 | Bos taurus | 27% | 100% |
Q4R8B6 | Macaca fascicularis | 28% | 100% |
Q5R9C1 | Pongo abelii | 27% | 100% |
Q6DTY7 | Mus musculus | 28% | 100% |
Q8TFH0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q91309 | Lithobates catesbeianus | 27% | 100% |
Q9UTE1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
V5DR58 | Trypanosoma cruzi | 55% | 97% |