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. | yes | yes: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 8 |
GO:0005737 | cytoplasm | 2 | 8 |
GO:0030015 | CCR4-NOT core complex | 3 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0140535 | intracellular protein-containing complex | 2 | 8 |
GO:0000932 | P-body | 5 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
Related structures:
AlphaFold database: E9AXR6
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 8 |
GO:0009889 | regulation of biosynthetic process | 4 | 8 |
GO:0010468 | regulation of gene expression | 5 | 8 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 8 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 8 |
GO:0019222 | regulation of metabolic process | 3 | 8 |
GO:0031323 | regulation of cellular metabolic process | 4 | 8 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 8 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 8 |
GO:0051252 | regulation of RNA metabolic process | 5 | 8 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0080090 | regulation of primary metabolic process | 4 | 8 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 8 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 8 |
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 | 114 | 118 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.406 |
CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.910 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.406 |
DEG_COP1_1 | 440 | 449 | PF00400 | 0.585 |
DEG_SCF_FBW7_1 | 472 | 478 | PF00400 | 0.776 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.775 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.789 |
DEG_SPOP_SBC_1 | 606 | 610 | PF00917 | 0.606 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.770 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 514 | 523 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 308 | 311 | PF00134 | 0.788 |
DOC_CYCLIN_yCln2_LP_2 | 467 | 473 | PF00134 | 0.793 |
DOC_CYCLIN_yCln2_LP_2 | 487 | 493 | PF00134 | 0.539 |
DOC_MAPK_gen_1 | 229 | 236 | PF00069 | 0.749 |
DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 229 | 236 | PF00069 | 0.743 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.788 |
DOC_PP2B_LxvP_1 | 467 | 470 | PF13499 | 0.780 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.657 |
DOC_SPAK_OSR1_1 | 351 | 355 | PF12202 | 0.569 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.834 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.817 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.858 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.613 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.808 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.606 |
DOC_USP7_UBL2_3 | 502 | 506 | PF12436 | 0.741 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.606 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.832 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.815 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.816 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.685 |
LIG_14-3-3_CanoR_1 | 615 | 621 | PF00244 | 0.606 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.675 |
LIG_BIR_III_2 | 538 | 542 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.792 |
LIG_BRCT_BRCA1_1 | 616 | 620 | PF00533 | 0.606 |
LIG_EVH1_1 | 491 | 495 | PF00568 | 0.819 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.795 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.735 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.899 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.809 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.811 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.599 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.779 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.610 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.595 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.582 |
LIG_Integrin_isoDGR_2 | 147 | 149 | PF01839 | 0.406 |
LIG_LIR_Apic_2 | 221 | 226 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 555 | 565 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 617 | 623 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 575 | 579 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 638 | 642 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.606 |
LIG_PCNA_PIPBox_1 | 559 | 568 | PF02747 | 0.592 |
LIG_PCNA_yPIPBox_3 | 554 | 566 | PF02747 | 0.592 |
LIG_Pex14_2 | 623 | 627 | PF04695 | 0.567 |
LIG_PTAP_UEV_1 | 446 | 451 | PF05743 | 0.578 |
LIG_PTB_Apo_2 | 65 | 72 | PF02174 | 0.606 |
LIG_PTB_Phospho_1 | 65 | 71 | PF10480 | 0.606 |
LIG_REV1ctd_RIR_1 | 172 | 180 | PF16727 | 0.657 |
LIG_SH2_NCK_1 | 531 | 535 | PF00017 | 0.606 |
LIG_SH2_SRC | 531 | 534 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 140 | 143 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 542 | 545 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 570 | 573 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.629 |
LIG_SH3_1 | 229 | 235 | PF00018 | 0.741 |
LIG_SH3_1 | 399 | 405 | PF00018 | 0.810 |
LIG_SH3_1 | 527 | 533 | PF00018 | 0.606 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.763 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.781 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.771 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.803 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.838 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.818 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.586 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.538 |
LIG_SUMO_SIM_anti_2 | 210 | 216 | PF11976 | 0.657 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.657 |
LIG_TRAF2_1 | 395 | 398 | PF00917 | 0.810 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.606 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.657 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.567 |
MOD_CDK_SPK_2 | 245 | 250 | PF00069 | 0.796 |
MOD_CDK_SPK_2 | 269 | 274 | PF00069 | 0.773 |
MOD_CDK_SPK_2 | 501 | 506 | PF00069 | 0.746 |
MOD_CDK_SPxK_1 | 501 | 507 | PF00069 | 0.737 |
MOD_CDK_SPxxK_3 | 377 | 384 | PF00069 | 0.788 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.782 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.707 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.406 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.606 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.764 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.861 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.762 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.606 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.867 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.606 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.406 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.379 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.387 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.789 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.533 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.406 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.736 |
MOD_GlcNHglycan | 456 | 460 | PF01048 | 0.796 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.833 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.575 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.811 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.678 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.833 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.872 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.570 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.777 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.592 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.584 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.374 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.680 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.672 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.606 |
MOD_NEK2_2 | 616 | 621 | PF00069 | 0.606 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.760 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.707 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.606 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.606 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.757 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.426 |
MOD_Plk_2-3 | 215 | 221 | PF00069 | 0.606 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.647 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.606 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.820 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.582 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.657 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.606 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.742 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.753 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.746 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.829 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.764 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.790 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.816 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.765 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.819 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.676 |
MOD_SUMO_for_1 | 175 | 178 | PF00179 | 0.657 |
MOD_SUMO_for_1 | 48 | 51 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 221 | 230 | PF00179 | 0.739 |
MOD_SUMO_rev_2 | 237 | 246 | PF00179 | 0.770 |
MOD_SUMO_rev_2 | 380 | 386 | PF00179 | 0.845 |
MOD_SUMO_rev_2 | 45 | 55 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 633 | 642 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 95 | 100 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.567 |
TRG_DiLeu_LyEn_5 | 10 | 15 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.567 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.601 |
TRG_NES_CRM1_1 | 199 | 215 | PF08389 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMJ8 | Leptomonas seymouri | 67% | 96% |
A0A3S5H7F0 | Leishmania donovani | 93% | 100% |
A4HE86 | Leishmania braziliensis | 86% | 99% |
A4I1N2 | Leishmania infantum | 93% | 100% |
C9ZK81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
Q4Q9Q5 | Leishmania major | 93% | 99% |