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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030015 | CCR4-NOT core complex | 3 | 5 |
GO:0032991 | protein-containing complex | 1 | 5 |
GO:0140535 | intracellular protein-containing complex | 2 | 5 |
GO:0000932 | P-body | 5 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WRX6
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 5 |
GO:0009889 | regulation of biosynthetic process | 4 | 5 |
GO:0010468 | regulation of gene expression | 5 | 5 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 5 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 5 |
GO:0019222 | regulation of metabolic process | 3 | 5 |
GO:0031323 | regulation of cellular metabolic process | 4 | 5 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 5 |
GO:0050789 | regulation of biological process | 2 | 5 |
GO:0050794 | regulation of cellular process | 3 | 5 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 5 |
GO:0051252 | regulation of RNA metabolic process | 5 | 5 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 5 |
GO:0065007 | biological regulation | 1 | 5 |
GO:0080090 | regulation of primary metabolic process | 4 | 5 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 5 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 5 |
GO:0000289 | nuclear-transcribed mRNA poly(A) tail shortening | 8 | 1 |
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006401 | RNA catabolic process | 5 | 1 |
GO:0006402 | mRNA catabolic process | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010629 | negative regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.703 |
CLV_C14_Caspase3-7 | 471 | 475 | PF00656 | 0.542 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.739 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.739 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.743 |
DEG_COP1_1 | 322 | 329 | PF00400 | 0.800 |
DOC_MAPK_gen_1 | 127 | 135 | PF00069 | 0.742 |
DOC_MAPK_JIP1_4 | 403 | 409 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 312 | 320 | PF00069 | 0.783 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.752 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.743 |
DOC_PP4_FxxP_1 | 25 | 28 | PF00568 | 0.849 |
DOC_PP4_FxxP_1 | 393 | 396 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.856 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.593 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.731 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.523 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.845 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.852 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.637 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.871 |
LIG_eIF4E_1 | 305 | 311 | PF01652 | 0.718 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.803 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.588 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.672 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.706 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.632 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.542 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.711 |
LIG_LIR_Apic_2 | 23 | 28 | PF02991 | 0.855 |
LIG_LIR_Apic_2 | 386 | 391 | PF02991 | 0.711 |
LIG_LIR_Apic_2 | 392 | 396 | PF02991 | 0.427 |
LIG_LIR_Apic_2 | 397 | 402 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 348 | 358 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 411 | 420 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 480 | 488 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.516 |
LIG_MYND_1 | 236 | 240 | PF01753 | 0.680 |
LIG_PCNA_yPIPBox_3 | 198 | 209 | PF02747 | 0.754 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.632 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.632 |
LIG_SH2_PTP2 | 388 | 391 | PF00017 | 0.701 |
LIG_SH2_SRC | 325 | 328 | PF00017 | 0.793 |
LIG_SH2_STAP1 | 385 | 389 | PF00017 | 0.722 |
LIG_SH2_STAT3 | 176 | 179 | PF00017 | 0.766 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.793 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.632 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.835 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.752 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.624 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.446 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.632 |
LIG_SH3_4 | 401 | 408 | PF00018 | 0.632 |
LIG_SUMO_SIM_anti_2 | 109 | 114 | PF11976 | 0.716 |
LIG_TRAF2_1 | 516 | 519 | PF00917 | 0.691 |
LIG_WRC_WIRS_1 | 409 | 414 | PF05994 | 0.632 |
LIG_WW_2 | 316 | 319 | PF00397 | 0.787 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.632 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.727 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.754 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.788 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.693 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.632 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.712 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.738 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.749 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.805 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.792 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.632 |
MOD_GlcNHglycan | 508 | 513 | PF01048 | 0.666 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.826 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.612 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.735 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.762 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.692 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.650 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.704 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.632 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.779 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.757 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.533 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.828 |
MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.680 |
MOD_N-GLC_1 | 556 | 561 | PF02516 | 0.800 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.660 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.680 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.696 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.608 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.504 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.708 |
MOD_NEK2_2 | 481 | 486 | PF00069 | 0.632 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.763 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.510 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.768 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.727 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.382 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.632 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.731 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.754 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.705 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.849 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.678 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.539 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.632 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.671 |
MOD_Plk_2-3 | 461 | 467 | PF00069 | 0.632 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.857 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.663 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.632 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.632 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.400 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.845 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.808 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.852 |
MOD_SUMO_for_1 | 415 | 418 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 386 | 396 | PF00179 | 0.696 |
TRG_DiLeu_BaEn_1 | 509 | 514 | PF01217 | 0.677 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.712 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.632 |
TRG_ER_diArg_1 | 129 | 132 | PF00400 | 0.738 |
TRG_NLS_MonoCore_2 | 399 | 404 | PF00514 | 0.632 |
TRG_NLS_MonoExtC_3 | 399 | 404 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.740 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.734 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.432 |