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:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HUY1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.525 |
CLV_PCSK_PC7_1 | 528 | 534 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.592 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.537 |
DEG_APCC_DBOX_1 | 523 | 531 | PF00400 | 0.502 |
DEG_SPOP_SBC_1 | 196 | 200 | PF00917 | 0.574 |
DOC_CKS1_1 | 313 | 318 | PF01111 | 0.616 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.554 |
DOC_MAPK_gen_1 | 133 | 143 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 136 | 143 | PF00069 | 0.555 |
DOC_MAPK_NFAT4_5 | 136 | 144 | PF00069 | 0.555 |
DOC_PP1_RVXF_1 | 101 | 107 | PF00149 | 0.404 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.620 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.601 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 510 | 514 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 359 | 369 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 402 | 409 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 524 | 528 | PF00244 | 0.455 |
LIG_Actin_WH2_2 | 405 | 422 | PF00022 | 0.511 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.572 |
LIG_CaM_IQ_9 | 47 | 63 | PF13499 | 0.415 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.516 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.586 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.608 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.599 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.653 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.618 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.557 |
LIG_GBD_Chelix_1 | 487 | 495 | PF00786 | 0.451 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.476 |
LIG_LYPXL_SIV_4 | 81 | 89 | PF13949 | 0.484 |
LIG_LYPXL_yS_3 | 453 | 456 | PF13949 | 0.534 |
LIG_MYND_1 | 282 | 286 | PF01753 | 0.599 |
LIG_PDZ_Class_2 | 551 | 556 | PF00595 | 0.478 |
LIG_PTB_Apo_2 | 302 | 309 | PF02174 | 0.547 |
LIG_PTB_Phospho_1 | 302 | 308 | PF10480 | 0.542 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.553 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.360 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.527 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.583 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 385 | 394 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 518 | 524 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 228 | 236 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 332 | 340 | PF11976 | 0.550 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.440 |
LIG_TRAF2_1 | 543 | 546 | PF00917 | 0.502 |
LIG_TYR_ITIM | 534 | 539 | PF00017 | 0.551 |
MOD_CDK_SPK_2 | 9 | 14 | PF00069 | 0.783 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.533 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.667 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.667 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.454 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.623 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.538 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.584 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.656 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.767 |
MOD_GlcNHglycan | 73 | 77 | PF01048 | 0.541 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.627 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.506 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.700 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.566 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.674 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.596 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.555 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.618 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.709 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.536 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.616 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.596 |
MOD_NEK2_2 | 37 | 42 | PF00069 | 0.547 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.429 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.494 |
MOD_PKA_1 | 42 | 48 | PF00069 | 0.489 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.488 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.547 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.462 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.473 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.547 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.489 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.536 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.536 |
MOD_PKB_1 | 184 | 192 | PF00069 | 0.610 |
MOD_PKB_1 | 202 | 210 | PF00069 | 0.641 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.533 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.330 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.528 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.693 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.516 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.540 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.409 |
MOD_Plk_2-3 | 229 | 235 | PF00069 | 0.622 |
MOD_Plk_2-3 | 541 | 547 | PF00069 | 0.566 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.638 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.695 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.676 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.529 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.751 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.637 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.572 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.552 |
MOD_SUMO_for_1 | 118 | 121 | PF00179 | 0.520 |
MOD_SUMO_for_1 | 495 | 498 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 375 | 381 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 506 | 516 | PF00179 | 0.614 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.563 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_4 | 339 | 345 | PF01217 | 0.420 |
TRG_DiLeu_BaEn_4 | 506 | 512 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.504 |
TRG_ER_diArg_1 | 107 | 109 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.775 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 532 | 534 | PF00400 | 0.554 |
TRG_NES_CRM1_1 | 417 | 433 | PF08389 | 0.465 |
TRG_NES_CRM1_1 | 512 | 525 | PF08389 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 186 | 191 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 503 | 507 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P310 | Leptomonas seymouri | 53% | 100% |
A0A0S4IYQ0 | Bodo saltans | 25% | 100% |
A0A1X0NVG8 | Trypanosomatidae | 31% | 100% |
A0A3Q8IB95 | Leishmania donovani | 100% | 100% |
A0A3R7L4W3 | Trypanosoma rangeli | 34% | 100% |
A4H6J6 | Leishmania braziliensis | 81% | 100% |
E9ANL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QH07 | Leishmania major | 96% | 100% |
V5C199 | Trypanosoma cruzi | 32% | 100% |