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:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQC5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 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:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic 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:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003723 | RNA binding | 4 | 8 |
GO:0003743 | translation initiation factor activity | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0008135 | translation factor activity, RNA binding | 3 | 8 |
GO:0045182 | translation regulator activity | 1 | 8 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 182 | 188 | PF00089 | 0.276 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.406 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.507 |
CLV_PCSK_PC7_1 | 50 | 56 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 739 | 743 | PF00082 | 0.489 |
DEG_MDM2_SWIB_1 | 28 | 35 | PF02201 | 0.636 |
DEG_MDM2_SWIB_1 | 665 | 673 | PF02201 | 0.477 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.683 |
DOC_ANK_TNKS_1 | 439 | 446 | PF00023 | 0.866 |
DOC_CYCLIN_RxL_1 | 41 | 48 | PF00134 | 0.616 |
DOC_MAPK_DCC_7 | 54 | 64 | PF00069 | 0.662 |
DOC_MAPK_gen_1 | 12 | 22 | PF00069 | 0.698 |
DOC_MAPK_gen_1 | 217 | 226 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 119 | 126 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 55 | 64 | PF00069 | 0.662 |
DOC_MAPK_MEF2A_6 | 556 | 564 | PF00069 | 0.409 |
DOC_MAPK_RevD_3 | 264 | 279 | PF00069 | 0.606 |
DOC_MAPK_RevD_3 | 40 | 55 | PF00069 | 0.449 |
DOC_MAPK_RevD_3 | 60 | 75 | PF00069 | 0.615 |
DOC_PP1_RVXF_1 | 318 | 325 | PF00149 | 0.569 |
DOC_PP2B_LxvP_1 | 650 | 653 | PF13499 | 0.598 |
DOC_PP4_FxxP_1 | 474 | 477 | PF00568 | 0.731 |
DOC_PP4_MxPP_1 | 468 | 471 | PF00568 | 0.743 |
DOC_PP4_MxPP_1 | 486 | 489 | PF00568 | 0.669 |
DOC_SPAK_OSR1_1 | 323 | 327 | PF12202 | 0.606 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.811 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.606 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 307 | 316 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 595 | 600 | PF00244 | 0.453 |
LIG_AP2alpha_1 | 197 | 201 | PF02296 | 0.606 |
LIG_APCC_ABBAyCdc20_2 | 737 | 743 | PF00400 | 0.678 |
LIG_BIR_III_4 | 721 | 725 | PF00653 | 0.410 |
LIG_BRCT_BRCA1_1 | 584 | 588 | PF00533 | 0.589 |
LIG_CtBP_PxDLS_1 | 427 | 431 | PF00389 | 0.766 |
LIG_deltaCOP1_diTrp_1 | 331 | 337 | PF00928 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 660 | 665 | PF00928 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 667 | 676 | PF00928 | 0.445 |
LIG_EH1_1 | 323 | 331 | PF00400 | 0.606 |
LIG_EVH1_2 | 470 | 474 | PF00568 | 0.792 |
LIG_EVH1_2 | 477 | 481 | PF00568 | 0.809 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.624 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.584 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.645 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.671 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.525 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.520 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.476 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.614 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.606 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.593 |
LIG_Integrin_isoDGR_2 | 183 | 185 | PF01839 | 0.457 |
LIG_Integrin_RGD_1 | 433 | 435 | PF01839 | 0.904 |
LIG_LIR_Apic_2 | 466 | 470 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 30 | 40 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 454 | 463 | PF02991 | 0.749 |
LIG_LIR_Gen_1 | 627 | 636 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 662 | 673 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 96 | 107 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 454 | 458 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 627 | 632 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 648 | 654 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 662 | 668 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 736 | 741 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.567 |
LIG_PCNA_yPIPBox_3 | 39 | 50 | PF02747 | 0.619 |
LIG_PDZ_Class_3 | 748 | 753 | PF00595 | 0.719 |
LIG_Pex14_1 | 661 | 665 | PF04695 | 0.494 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.606 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.628 |
LIG_Pex14_2 | 665 | 669 | PF04695 | 0.476 |
LIG_PTB_Apo_2 | 220 | 227 | PF02174 | 0.567 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.575 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.652 |
LIG_SH2_PTP2 | 561 | 564 | PF00017 | 0.348 |
LIG_SH2_PTP2 | 651 | 654 | PF00017 | 0.614 |
LIG_SH2_SRC | 561 | 564 | PF00017 | 0.435 |
LIG_SH2_SRC | 646 | 649 | PF00017 | 0.528 |
LIG_SH2_SRC | 719 | 722 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 597 | 601 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 617 | 621 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 646 | 649 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 719 | 722 | PF00017 | 0.642 |
LIG_SH3_1 | 467 | 473 | PF00018 | 0.714 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.577 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.606 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.639 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.796 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.796 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.769 |
LIG_SH3_3 | 675 | 681 | PF00018 | 0.482 |
LIG_Sin3_3 | 99 | 106 | PF02671 | 0.657 |
LIG_SUMO_SIM_anti_2 | 686 | 692 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 240 | 247 | PF11976 | 0.606 |
LIG_TRAF2_1 | 571 | 574 | PF00917 | 0.504 |
LIG_UBA3_1 | 272 | 278 | PF00899 | 0.572 |
LIG_UBA3_1 | 505 | 513 | PF00899 | 0.642 |
LIG_UBA3_1 | 690 | 698 | PF00899 | 0.557 |
MOD_CDC14_SPxK_1 | 510 | 513 | PF00782 | 0.473 |
MOD_CDK_SPK_2 | 253 | 258 | PF00069 | 0.657 |
MOD_CDK_SPxK_1 | 507 | 513 | PF00069 | 0.647 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.476 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.862 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.813 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.710 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.636 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.633 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.547 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.447 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.559 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.476 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.792 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.576 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.406 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.406 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.795 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.887 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.785 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.561 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.476 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.848 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.790 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.884 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.866 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.733 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.518 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.501 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.374 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.457 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.824 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.769 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.621 |
MOD_N-GLC_1 | 731 | 736 | PF02516 | 0.573 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.476 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.657 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.635 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.608 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.497 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.520 |
MOD_NEK2_1 | 712 | 717 | PF00069 | 0.631 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.690 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.768 |
MOD_PIKK_1 | 712 | 718 | PF00454 | 0.638 |
MOD_PK_1 | 409 | 415 | PF00069 | 0.628 |
MOD_PKA_1 | 565 | 571 | PF00069 | 0.568 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.582 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.559 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.835 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.657 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.624 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.758 |
MOD_Plk_2-3 | 569 | 575 | PF00069 | 0.605 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.657 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.606 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.533 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.530 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.567 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.658 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.726 |
MOD_SUMO_rev_2 | 429 | 439 | PF00179 | 0.708 |
MOD_SUMO_rev_2 | 496 | 506 | PF00179 | 0.615 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.657 |
TRG_DiLeu_BaEn_1 | 501 | 506 | PF01217 | 0.649 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.687 |
TRG_DiLeu_BaEn_4 | 177 | 183 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 651 | 654 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.600 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 320 | 323 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 576 | 581 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL6 | Leptomonas seymouri | 66% | 100% |
A0A3Q8IJA9 | Leishmania donovani | 83% | 99% |
A4IE18 | Leishmania infantum | 83% | 99% |
D0A8R4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AU41 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 98% |
Q4Q0F4 | Leishmania major | 82% | 100% |