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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IHC4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.582 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.665 |
CLV_Separin_Metazoa | 289 | 293 | PF03568 | 0.509 |
DEG_APCC_DBOX_1 | 411 | 419 | PF00400 | 0.599 |
DEG_COP1_1 | 187 | 197 | PF00400 | 0.597 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.274 |
DOC_CYCLIN_RxL_1 | 222 | 235 | PF00134 | 0.607 |
DOC_PP1_RVXF_1 | 433 | 439 | PF00149 | 0.617 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.491 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.405 |
DOC_USP7_UBL2_3 | 228 | 232 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 69 | 73 | PF12436 | 0.349 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 258 | 268 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 302 | 308 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.599 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.424 |
LIG_deltaCOP1_diTrp_1 | 142 | 149 | PF00928 | 0.330 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.355 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.607 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.543 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.512 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.409 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.633 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.735 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.651 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.611 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.619 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.528 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.617 |
LIG_LIR_Apic_2 | 105 | 110 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 487 | 498 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 487 | 493 | PF02991 | 0.531 |
LIG_NRBOX | 201 | 207 | PF00104 | 0.654 |
LIG_PCNA_PIPBox_1 | 381 | 390 | PF02747 | 0.468 |
LIG_PCNA_yPIPBox_3 | 222 | 231 | PF02747 | 0.499 |
LIG_Pex14_1 | 145 | 149 | PF04695 | 0.224 |
LIG_SH2_CRK | 107 | 111 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 107 | 111 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.543 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.316 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.652 |
LIG_SUMO_SIM_anti_2 | 309 | 316 | PF11976 | 0.487 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.597 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.515 |
LIG_UBA3_1 | 415 | 419 | PF00899 | 0.410 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.722 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.621 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.495 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.519 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.683 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.563 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.349 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.619 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.453 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.395 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.322 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.320 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.691 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.692 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.511 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.447 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.404 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.424 |
MOD_GlcNHglycan | 187 | 191 | PF01048 | 0.715 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.615 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.585 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.687 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.701 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.493 |
MOD_GlcNHglycan | 78 | 82 | PF01048 | 0.150 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.540 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.683 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.570 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.586 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.654 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.694 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.409 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.654 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.491 |
MOD_N-GLC_2 | 28 | 30 | PF02516 | 0.349 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.503 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.568 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.610 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.581 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.349 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.527 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.562 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.550 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.600 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.648 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.349 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.366 |
MOD_NEK2_2 | 223 | 228 | PF00069 | 0.530 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.621 |
MOD_OFUCOSY | 425 | 431 | PF10250 | 0.418 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.482 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.522 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.349 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.601 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.545 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.568 |
MOD_PKB_1 | 505 | 513 | PF00069 | 0.515 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.564 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.682 |
MOD_Plk_2-3 | 397 | 403 | PF00069 | 0.591 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.296 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.736 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.545 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.591 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.552 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.511 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.458 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.266 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.708 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.349 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.493 |
MOD_SUMO_for_1 | 439 | 442 | PF00179 | 0.599 |
MOD_SUMO_rev_2 | 66 | 74 | PF00179 | 0.427 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 521 | 526 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HV83 | Leptomonas seymouri | 52% | 78% |
A0A1X0NVA0 | Trypanosomatidae | 33% | 78% |
A0A3R7LGF2 | Trypanosoma rangeli | 31% | 81% |
A4H9U9 | Leishmania braziliensis | 84% | 100% |
A4HUS1 | Leishmania infantum | 100% | 100% |
D0A7P2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 81% |
E9ANF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QH71 | Leishmania major | 96% | 100% |
V5BB15 | Trypanosoma cruzi | 38% | 81% |