Structural Proteins, dynein
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005858 | axonemal dynein complex | 4 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0030286 | dynein complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036157 | outer dynein arm | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X5B2
Term | Name | Level | Count |
---|---|---|---|
GO:0003341 | cilium movement | 4 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0036158 | outer dynein arm assembly | 7 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0070286 | axonemal dynein complex assembly | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 1 |
GO:0003777 | microtubule motor activity | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0045503 | dynein light chain binding | 3 | 1 |
GO:0045504 | dynein heavy chain binding | 3 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 580 | 584 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 536 | 540 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 165 | 167 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.429 |
CLV_PCSK_PC7_1 | 534 | 540 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.465 |
DEG_APCC_DBOX_1 | 323 | 331 | PF00400 | 0.546 |
DEG_SCF_FBW7_2 | 546 | 553 | PF00400 | 0.579 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.441 |
DOC_CKS1_1 | 453 | 458 | PF01111 | 0.392 |
DOC_MAPK_gen_1 | 99 | 108 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 452 | 460 | PF00069 | 0.397 |
DOC_PP1_RVXF_1 | 184 | 190 | PF00149 | 0.432 |
DOC_PP1_RVXF_1 | 399 | 405 | PF00149 | 0.442 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.542 |
DOC_USP7_UBL2_3 | 563 | 567 | PF12436 | 0.491 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.441 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 358 | 368 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 452 | 456 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 536 | 546 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 548 | 557 | PF00244 | 0.525 |
LIG_Actin_WH2_2 | 437 | 454 | PF00022 | 0.369 |
LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.359 |
LIG_BRCT_BRCA1_1 | 456 | 460 | PF00533 | 0.525 |
LIG_deltaCOP1_diTrp_1 | 266 | 273 | PF00928 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 397 | 404 | PF00928 | 0.322 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.480 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.441 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.386 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.507 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.620 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.517 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.528 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.556 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.439 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.433 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.346 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.525 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.602 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.642 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.462 |
LIG_LIR_Apic_2 | 5 | 11 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 200 | 211 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 389 | 400 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 410 | 421 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 441 | 451 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 410 | 416 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 441 | 446 | PF02991 | 0.369 |
LIG_MLH1_MIPbox_1 | 388 | 392 | PF16413 | 0.359 |
LIG_Pex14_1 | 403 | 407 | PF04695 | 0.339 |
LIG_Pex14_2 | 388 | 392 | PF04695 | 0.359 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.403 |
LIG_PTB_Apo_2 | 382 | 389 | PF02174 | 0.400 |
LIG_REV1ctd_RIR_1 | 433 | 443 | PF16727 | 0.345 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.407 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 8 | 12 | PF00017 | 0.629 |
LIG_SH2_PTP2 | 443 | 446 | PF00017 | 0.489 |
LIG_SH2_SRC | 443 | 446 | PF00017 | 0.435 |
LIG_SH2_STAT3 | 334 | 337 | PF00017 | 0.397 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.437 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.538 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.457 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.482 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.416 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.423 |
LIG_SUMO_SIM_par_1 | 280 | 287 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 489 | 494 | PF11976 | 0.393 |
LIG_TRAF2_1 | 141 | 144 | PF00917 | 0.672 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.254 |
LIG_TRAF2_1 | 551 | 554 | PF00917 | 0.677 |
LIG_TRAF2_1 | 578 | 581 | PF00917 | 0.553 |
LIG_TYR_ITIM | 182 | 187 | PF00017 | 0.378 |
LIG_WRC_WIRS_1 | 413 | 418 | PF05994 | 0.369 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.457 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.458 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.425 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.663 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.585 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.456 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.553 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.523 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.367 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.524 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.608 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.585 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.519 |
MOD_Cter_Amidation | 176 | 179 | PF01082 | 0.422 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.258 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.393 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.623 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.468 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.569 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.418 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.370 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.360 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.398 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.368 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.606 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.560 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.635 |
MOD_LATS_1 | 577 | 583 | PF00433 | 0.514 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.602 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.359 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.431 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.508 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.357 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.330 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.412 |
MOD_NEK2_2 | 466 | 471 | PF00069 | 0.482 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.578 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.441 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.628 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.524 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.356 |
MOD_PKA_1 | 538 | 544 | PF00069 | 0.526 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.407 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.522 |
MOD_PKB_1 | 536 | 544 | PF00069 | 0.511 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.551 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.571 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.367 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.437 |
MOD_Plk_2-3 | 513 | 519 | PF00069 | 0.427 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.469 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.386 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.365 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.366 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.464 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.473 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.422 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.345 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.397 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.394 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.583 |
MOD_SUMO_rev_2 | 160 | 167 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 405 | 410 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 87 | 95 | PF00179 | 0.456 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 536 | 539 | PF00400 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P997 | Leptomonas seymouri | 85% | 100% |
A0A0N1HUS1 | Leptomonas seymouri | 23% | 100% |
A0A0N1I862 | Leptomonas seymouri | 25% | 88% |
A0A0S4IN87 | Bodo saltans | 29% | 78% |
A0A0S4INJ7 | Bodo saltans | 25% | 93% |
A0A0S4JPP6 | Bodo saltans | 24% | 78% |
A0A1X0NJ43 | Trypanosomatidae | 24% | 89% |
A0A1X0NUK4 | Trypanosomatidae | 70% | 100% |
A0A1X0P0W1 | Trypanosomatidae | 24% | 100% |
A0A3S5IRX8 | Trypanosoma rangeli | 23% | 100% |
A0A3S7X1Z8 | Leishmania donovani | 24% | 100% |
A0A422P1D5 | Trypanosoma rangeli | 68% | 100% |
A2AC93 | Mus musculus | 42% | 96% |
A4HFT9 | Leishmania braziliensis | 25% | 76% |
A4HK88 | Leishmania braziliensis | 92% | 100% |
A4I447 | Leishmania infantum | 24% | 100% |
A4I7S3 | Leishmania infantum | 100% | 100% |
D0A634 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 74% |
D0A6Z5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 92% |
D0A9Y1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
E9ADL2 | Leishmania major | 25% | 100% |
E9AM69 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B2N1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
P27766 | Chlamydomonas reinhardtii | 42% | 100% |
Q16959 | Heliocidaris crassispina | 28% | 86% |
Q16960 | Heliocidaris crassispina | 44% | 100% |
Q32KS2 | Bos taurus | 24% | 86% |
Q4Q5H6 | Leishmania major | 98% | 100% |
Q4QR00 | Xenopus laevis | 43% | 100% |
Q5XIL8 | Rattus norvegicus | 25% | 85% |
Q66HC9 | Rattus norvegicus | 40% | 97% |
Q8C0M8 | Mus musculus | 25% | 86% |
Q9GZS0 | Homo sapiens | 40% | 99% |
Q9UI46 | Homo sapiens | 24% | 86% |
V5B145 | Trypanosoma cruzi | 69% | 100% |
V5BGF1 | Trypanosoma cruzi | 25% | 74% |
V5DSN6 | Trypanosoma cruzi | 24% | 90% |