A family of very long coiled-coil proteins, likely performing cytoskeletal functions.. Two varieties have evolved, one with an N-terminal FYVE domain (Non-TM) and another with a C-terminal PDZ domain (might be TM)
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: 3 |
NetGPI | no | yes: 0, no: 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HSF6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 784 | 786 | PF00675 | 0.468 |
CLV_PCSK_FUR_1 | 782 | 786 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 782 | 784 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 779 | 785 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.283 |
CLV_Separin_Metazoa | 60 | 64 | PF03568 | 0.420 |
DEG_SPOP_SBC_1 | 295 | 299 | PF00917 | 0.709 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.405 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.784 |
DOC_MAPK_DCC_7 | 171 | 181 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 171 | 181 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 174 | 183 | PF00069 | 0.366 |
DOC_PP1_RVXF_1 | 109 | 116 | PF00149 | 0.455 |
DOC_PP2B_LxvP_1 | 17 | 20 | PF13499 | 0.258 |
DOC_PP2B_PxIxI_1 | 177 | 183 | PF00149 | 0.283 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.694 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.382 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 771 | 776 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 131 | 141 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 240 | 249 | PF00244 | 0.782 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 329 | 338 | PF00244 | 0.813 |
LIG_14-3-3_CanoR_1 | 74 | 81 | PF00244 | 0.307 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.695 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.355 |
LIG_eIF4E_1 | 370 | 376 | PF01652 | 0.685 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.403 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.291 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.745 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.785 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.622 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.685 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.330 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.812 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.460 |
LIG_FHA_2 | 741 | 747 | PF00498 | 0.550 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.692 |
LIG_LIR_Apic_2 | 777 | 781 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 147 | 158 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 46 | 56 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.328 |
LIG_Pex14_2 | 86 | 90 | PF04695 | 0.305 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.466 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.434 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.770 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.801 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.754 |
LIG_SH3_3 | 790 | 796 | PF00018 | 0.630 |
LIG_SH3_CIN85_PxpxPR_1 | 401 | 406 | PF14604 | 0.653 |
LIG_SH3_CIN85_PxpxPR_1 | 764 | 769 | PF14604 | 0.675 |
LIG_SUMO_SIM_par_1 | 27 | 33 | PF11976 | 0.316 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.659 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.639 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.657 |
LIG_TRAF2_1 | 516 | 519 | PF00917 | 0.670 |
LIG_TRAF2_1 | 549 | 552 | PF00917 | 0.657 |
LIG_TRAF2_1 | 582 | 585 | PF00917 | 0.733 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.654 |
LIG_TRAF2_1 | 648 | 651 | PF00917 | 0.666 |
LIG_TRAF2_1 | 681 | 684 | PF00917 | 0.647 |
LIG_TRAF2_1 | 714 | 717 | PF00917 | 0.645 |
LIG_TRAF2_1 | 747 | 750 | PF00917 | 0.639 |
LIG_TRAF2_1 | 813 | 816 | PF00917 | 0.641 |
LIG_TRAF2_2 | 276 | 281 | PF00917 | 0.702 |
LIG_TYR_ITIM | 148 | 153 | PF00017 | 0.436 |
LIG_WW_3 | 60 | 64 | PF00397 | 0.420 |
MOD_CDK_SPK_2 | 235 | 240 | PF00069 | 0.785 |
MOD_CDK_SPK_2 | 771 | 776 | PF00069 | 0.668 |
MOD_CDK_SPxxK_3 | 282 | 289 | PF00069 | 0.706 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.445 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.776 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.706 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.717 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.717 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.387 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.316 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.654 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.462 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.551 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.627 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.641 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.569 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.302 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.500 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.509 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.426 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.785 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.674 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.822 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.709 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.754 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.366 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.648 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.691 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.631 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.628 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.553 |
MOD_N-GLC_2 | 157 | 159 | PF02516 | 0.608 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.695 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.436 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.697 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.711 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.397 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.306 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.736 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.790 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.350 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.308 |
MOD_PIKK_1 | 795 | 801 | PF00454 | 0.578 |
MOD_PK_1 | 118 | 124 | PF00069 | 0.430 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.258 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.710 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.750 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.715 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.381 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.616 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.703 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.743 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.608 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.630 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.632 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.652 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.646 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.627 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.405 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.625 |
MOD_Plk_1 | 694 | 700 | PF00069 | 0.610 |
MOD_Plk_1 | 727 | 733 | PF00069 | 0.611 |
MOD_Plk_1 | 826 | 832 | PF00069 | 0.613 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.316 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.686 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.649 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.385 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.728 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.675 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.704 |
MOD_ProDKin_1 | 771 | 777 | PF00069 | 0.665 |
MOD_SUMO_for_1 | 303 | 306 | PF00179 | 0.703 |
MOD_SUMO_rev_2 | 251 | 256 | PF00179 | 0.685 |
TRG_DiLeu_BaEn_4 | 419 | 425 | PF01217 | 0.620 |
TRG_DiLeu_BaEn_4 | 452 | 458 | PF01217 | 0.648 |
TRG_DiLeu_BaEn_4 | 485 | 491 | PF01217 | 0.666 |
TRG_DiLeu_BaEn_4 | 518 | 524 | PF01217 | 0.677 |
TRG_DiLeu_BaEn_4 | 551 | 557 | PF01217 | 0.626 |
TRG_DiLeu_BaEn_4 | 584 | 590 | PF01217 | 0.734 |
TRG_DiLeu_BaEn_4 | 617 | 623 | PF01217 | 0.622 |
TRG_DiLeu_BaEn_4 | 650 | 656 | PF01217 | 0.632 |
TRG_DiLeu_BaEn_4 | 683 | 689 | PF01217 | 0.611 |
TRG_DiLeu_BaEn_4 | 716 | 722 | PF01217 | 0.613 |
TRG_DiLeu_BaEn_4 | 749 | 755 | PF01217 | 0.655 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 768 | 771 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 781 | 784 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 839 | 842 | PF00400 | 0.564 |
TRG_NLS_Bipartite_1 | 381 | 403 | PF00514 | 0.706 |
TRG_NLS_MonoCore_2 | 398 | 403 | PF00514 | 0.674 |
TRG_NLS_MonoExtC_3 | 397 | 402 | PF00514 | 0.679 |
TRG_NLS_MonoExtN_4 | 324 | 330 | PF00514 | 0.732 |
TRG_NLS_MonoExtN_4 | 397 | 403 | PF00514 | 0.713 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5G8 | Leishmania donovani | 92% | 89% |
Q4QJH9 | Leishmania major | 66% | 69% |