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: A4HE86
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 | 0.581 |
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.582 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.333 |
CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.896 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.343 |
DEG_Kelch_Keap1_1 | 315 | 320 | PF01344 | 0.583 |
DEG_SCF_FBW7_1 | 472 | 478 | PF00400 | 0.847 |
DEG_SPOP_SBC_1 | 248 | 252 | PF00917 | 0.575 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.574 |
DEG_SPOP_SBC_1 | 602 | 606 | PF00917 | 0.545 |
DOC_CKS1_1 | 441 | 446 | PF01111 | 0.581 |
DOC_CKS1_1 | 460 | 465 | PF01111 | 0.606 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.832 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 510 | 519 | PF00134 | 0.377 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.600 |
DOC_MAPK_gen_1 | 228 | 235 | PF00069 | 0.651 |
DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.522 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.581 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.624 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.522 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.836 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.661 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.742 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.533 |
DOC_USP7_UBL2_3 | 498 | 502 | PF12436 | 0.550 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.533 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 396 | 402 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 611 | 617 | PF00244 | 0.533 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 612 | 616 | PF00533 | 0.533 |
LIG_EVH1_1 | 487 | 491 | PF00568 | 0.639 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.525 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.551 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.629 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.699 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.671 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.802 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.515 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.647 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.642 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.794 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.539 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.520 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.507 |
LIG_Integrin_isoDGR_2 | 147 | 149 | PF01839 | 0.333 |
LIG_LIR_Apic_2 | 220 | 225 | PF02991 | 0.522 |
LIG_LIR_Apic_2 | 367 | 371 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 551 | 561 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 613 | 619 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 571 | 575 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 634 | 638 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.533 |
LIG_MAD2 | 363 | 371 | PF02301 | 0.557 |
LIG_Pex14_2 | 619 | 623 | PF04695 | 0.493 |
LIG_PTB_Apo_2 | 65 | 72 | PF02174 | 0.533 |
LIG_PTB_Phospho_1 | 65 | 71 | PF10480 | 0.533 |
LIG_REV1ctd_RIR_1 | 171 | 179 | PF16727 | 0.522 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.533 |
LIG_SH2_SRC | 527 | 530 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 140 | 143 | PF00017 | 0.558 |
LIG_SH2_STAT3 | 538 | 541 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 566 | 569 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.556 |
LIG_SH3_1 | 523 | 529 | PF00018 | 0.533 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.594 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.538 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.570 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.654 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.680 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.650 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.731 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.748 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 209 | 215 | PF11976 | 0.522 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.612 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.533 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.522 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.493 |
MOD_CDK_SPK_2 | 244 | 249 | PF00069 | 0.691 |
MOD_CDK_SPK_2 | 497 | 502 | PF00069 | 0.556 |
MOD_CDK_SPxK_1 | 497 | 503 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 374 | 381 | PF00069 | 0.659 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.675 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.569 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.653 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.689 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.643 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.406 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.533 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.662 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.654 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.662 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.533 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.694 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.786 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.533 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.333 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.321 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.360 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.601 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.333 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.656 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.533 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.794 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.778 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.752 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.671 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.841 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.797 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.658 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.704 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.545 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.508 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.298 |
MOD_N-GLC_1 | 433 | 438 | PF02516 | 0.551 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.612 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.526 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.533 |
MOD_NEK2_2 | 612 | 617 | PF00069 | 0.533 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.567 |
MOD_PK_1 | 228 | 234 | PF00069 | 0.524 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.533 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.533 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.637 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.322 |
MOD_Plk_2-3 | 187 | 193 | PF00069 | 0.525 |
MOD_Plk_2-3 | 214 | 220 | PF00069 | 0.558 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.603 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.533 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.648 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.556 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.507 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.522 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.533 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.637 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.643 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.617 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.609 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.727 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.689 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.683 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.627 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.605 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.652 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.735 |
MOD_SUMO_for_1 | 174 | 177 | PF00179 | 0.522 |
MOD_SUMO_for_1 | 48 | 51 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 220 | 229 | PF00179 | 0.669 |
MOD_SUMO_rev_2 | 236 | 245 | PF00179 | 0.667 |
MOD_SUMO_rev_2 | 45 | 55 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 629 | 638 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 95 | 100 | PF00179 | 0.533 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.493 |
TRG_DiLeu_LyEn_5 | 10 | 15 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.533 |
TRG_NES_CRM1_1 | 198 | 214 | PF08389 | 0.612 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMJ8 | Leptomonas seymouri | 65% | 95% |
A0A3S5H7F0 | Leishmania donovani | 87% | 100% |
A4I1N2 | Leishmania infantum | 87% | 100% |
C9ZK81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AXR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4Q9Q5 | Leishmania major | 87% | 99% |