Uncharacterized Protein, Uncharacterized
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005858 | axonemal dynein complex | 4 | 12 |
GO:0005875 | microtubule associated complex | 2 | 12 |
GO:0030286 | dynein complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AHZ1
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 12 |
GO:0070286 | axonemal dynein complex assembly | 6 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
GO:0003352 | regulation of cilium movement | 6 | 1 |
GO:0032886 | regulation of microtubule-based process | 4 | 1 |
GO:0048870 | cell motility | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0060285 | cilium-dependent cell motility | 4 | 1 |
GO:0060632 | regulation of microtubule-based movement | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.461 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.228 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.228 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 552 | 558 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.565 |
DEG_APCC_KENBOX_2 | 299 | 303 | PF00400 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 400 | 406 | PF00134 | 0.379 |
DOC_MAPK_gen_1 | 143 | 150 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 364 | 373 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 143 | 150 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 143 | 151 | PF00069 | 0.370 |
DOC_PP1_SILK_1 | 446 | 451 | PF00149 | 0.499 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.378 |
DOC_PP2B_LxvP_1 | 630 | 633 | PF13499 | 0.441 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.395 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.470 |
DOC_USP7_UBL2_3 | 365 | 369 | PF12436 | 0.451 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 180 | 187 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 261 | 270 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 287 | 291 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 489 | 497 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 635 | 643 | PF00244 | 0.485 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.513 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 |
LIG_BIR_III_2 | 3 | 7 | PF00653 | 0.492 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.576 |
LIG_CaM_IQ_9 | 191 | 207 | PF13499 | 0.387 |
LIG_eIF4E_1 | 631 | 637 | PF01652 | 0.487 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.417 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.595 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.410 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.556 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.454 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.453 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.382 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.489 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.540 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.539 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.619 |
LIG_LIR_Apic_2 | 629 | 634 | PF02991 | 0.496 |
LIG_LIR_Apic_2 | 642 | 646 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 368 | 376 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.464 |
LIG_NRBOX | 319 | 325 | PF00104 | 0.519 |
LIG_PCNA_yPIPBox_3 | 310 | 324 | PF02747 | 0.423 |
LIG_PCNA_yPIPBox_3 | 608 | 618 | PF02747 | 0.421 |
LIG_SH2_CRK | 631 | 635 | PF00017 | 0.499 |
LIG_SH2_GRB2like | 621 | 624 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 643 | 647 | PF00017 | 0.518 |
LIG_SH2_PTP2 | 161 | 164 | PF00017 | 0.513 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.372 |
LIG_SH2_SRC | 631 | 634 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 628 | 632 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 186 | 189 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 230 | 233 | PF00017 | 0.470 |
LIG_SH2_STAT3 | 290 | 293 | PF00017 | 0.403 |
LIG_SH2_STAT3 | 590 | 593 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.452 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 505 | 513 | PF11976 | 0.588 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.435 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.488 |
LIG_TRAF2_1 | 413 | 416 | PF00917 | 0.582 |
LIG_TRAF2_1 | 530 | 533 | PF00917 | 0.485 |
LIG_TRAF2_1 | 6 | 9 | PF00917 | 0.522 |
LIG_TYR_ITIM | 394 | 399 | PF00017 | 0.473 |
LIG_TYR_ITIM | 497 | 502 | PF00017 | 0.428 |
LIG_UBA3_1 | 444 | 450 | PF00899 | 0.417 |
LIG_WRC_WIRS_1 | 359 | 364 | PF05994 | 0.409 |
LIG_WW_3 | 632 | 636 | PF00397 | 0.565 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.460 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.592 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.333 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.467 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.592 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.543 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.267 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.409 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.564 |
MOD_CK2_1 | 641 | 647 | PF00069 | 0.656 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.534 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.335 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.335 |
MOD_GlcNHglycan | 98 | 102 | PF01048 | 0.228 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.590 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.430 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.323 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.575 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.513 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.495 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.592 |
MOD_N-GLC_1 | 487 | 492 | PF02516 | 0.535 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.590 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.522 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.503 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.522 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.601 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.395 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.351 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.422 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.340 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.444 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.492 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.428 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.569 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.494 |
MOD_PIKK_1 | 585 | 591 | PF00454 | 0.486 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.665 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.461 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.453 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.360 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.431 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.541 |
MOD_PKB_1 | 16 | 24 | PF00069 | 0.495 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.516 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.415 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.494 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.377 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.385 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.607 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 210 | 219 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 229 | 239 | PF00179 | 0.295 |
MOD_SUMO_rev_2 | 42 | 51 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 526 | 536 | PF00179 | 0.517 |
TRG_DiLeu_BaEn_1 | 135 | 140 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_1 | 171 | 176 | PF01217 | 0.601 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_1 | 613 | 618 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.472 |
TRG_NES_CRM1_1 | 137 | 152 | PF08389 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAH6 | Leptomonas seymouri | 69% | 100% |
A0A0S4J8E8 | Bodo saltans | 40% | 100% |
A0A1X0NL92 | Trypanosomatidae | 48% | 100% |
A0A3R7KG47 | Trypanosoma rangeli | 44% | 99% |
A0A3S7XCE4 | Leishmania donovani | 100% | 100% |
A4HQI2 | Leishmania braziliensis | 82% | 100% |
D0A3N0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AU95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
F1QRC1 | Danio rerio | 25% | 97% |
P0DL09 | Chlamydomonas reinhardtii | 27% | 93% |
Q32KY1 | Bos taurus | 25% | 91% |
Q3USS3 | Mus musculus | 26% | 86% |
Q4Q096 | Leishmania major | 95% | 100% |
Q5XI65 | Rattus norvegicus | 26% | 86% |
Q7T0Y4 | Xenopus laevis | 28% | 94% |
V5BD07 | Trypanosoma cruzi | 51% | 100% |