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: 5 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4H7T4
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 3 |
GO:0007018 | microtubule-based movement | 3 | 3 |
GO:0009987 | cellular process | 1 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 3 |
GO:0003777 | microtubule motor activity | 2 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005524 | ATP binding | 5 | 1 |
GO:0008017 | microtubule binding | 5 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1014 | 1018 | PF00656 | 0.407 |
CLV_C14_Caspase3-7 | 104 | 108 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 1049 | 1053 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.446 |
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.415 |
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.488 |
CLV_C14_Caspase3-7 | 433 | 437 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 559 | 563 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 601 | 605 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.414 |
CLV_C14_Caspase3-7 | 643 | 647 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 685 | 689 | PF00656 | 0.488 |
CLV_C14_Caspase3-7 | 727 | 731 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 769 | 773 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 811 | 815 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 853 | 857 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 895 | 899 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 937 | 941 | PF00656 | 0.422 |
CLV_C14_Caspase3-7 | 972 | 976 | PF00656 | 0.408 |
DEG_Nend_UBRbox_3 | 1 | 2 | PF02207 | 0.476 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 944 | 953 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 944 | 949 | PF02991 | 0.424 |
MOD_Plk_2-3 | 101 | 107 | PF00069 | 0.429 |
MOD_Plk_2-3 | 1011 | 1017 | PF00069 | 0.403 |
MOD_Plk_2-3 | 1046 | 1052 | PF00069 | 0.452 |
MOD_Plk_2-3 | 143 | 149 | PF00069 | 0.475 |
MOD_Plk_2-3 | 185 | 191 | PF00069 | 0.477 |
MOD_Plk_2-3 | 227 | 233 | PF00069 | 0.517 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.429 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.464 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.471 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.476 |
MOD_Plk_2-3 | 388 | 394 | PF00069 | 0.486 |
MOD_Plk_2-3 | 430 | 436 | PF00069 | 0.530 |
MOD_Plk_2-3 | 472 | 478 | PF00069 | 0.492 |
MOD_Plk_2-3 | 514 | 520 | PF00069 | 0.496 |
MOD_Plk_2-3 | 556 | 562 | PF00069 | 0.502 |
MOD_Plk_2-3 | 59 | 65 | PF00069 | 0.426 |
MOD_Plk_2-3 | 598 | 604 | PF00069 | 0.530 |
MOD_Plk_2-3 | 640 | 646 | PF00069 | 0.513 |
MOD_Plk_2-3 | 682 | 688 | PF00069 | 0.504 |
MOD_Plk_2-3 | 724 | 730 | PF00069 | 0.541 |
MOD_Plk_2-3 | 766 | 772 | PF00069 | 0.536 |
MOD_Plk_2-3 | 808 | 814 | PF00069 | 0.521 |
MOD_Plk_2-3 | 850 | 856 | PF00069 | 0.524 |
MOD_Plk_2-3 | 892 | 898 | PF00069 | 0.469 |
MOD_Plk_2-3 | 934 | 940 | PF00069 | 0.449 |
MOD_Plk_2-3 | 969 | 975 | PF00069 | 0.410 |
MOD_SUMO_rev_2 | 1008 | 1014 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 1043 | 1049 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 140 | 146 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 182 | 188 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 21 | 27 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 224 | 230 | PF00179 | 0.523 |
MOD_SUMO_rev_2 | 266 | 272 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 308 | 314 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 350 | 356 | PF00179 | 0.462 |
MOD_SUMO_rev_2 | 385 | 391 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 427 | 433 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 469 | 475 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 511 | 517 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 553 | 559 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 56 | 62 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 595 | 601 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 637 | 643 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 679 | 685 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 721 | 727 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 763 | 769 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 805 | 811 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 847 | 853 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 889 | 895 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 931 | 937 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 966 | 972 | PF00179 | 0.415 |
MOD_SUMO_rev_2 | 98 | 104 | PF00179 | 0.455 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 946 | 949 | PF00928 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4HBI8 | Leishmania braziliensis | 35% | 100% |
A4HW56 | Leishmania infantum | 73% | 100% |
A4I9N9 | Leishmania infantum | 33% | 80% |
A4IAN8 | Leishmania infantum | 32% | 69% |
E8NHK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E8NHN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AQ46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 89% |
Q54G05 | Dictyostelium discoideum | 24% | 71% |