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. | yes | 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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 5, no: 6 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0005793 | endoplasmic reticulum-Golgi intermediate compartment | 5 | 1 |
GO:0030134 | COPII-coated ER to Golgi transport vesicle | 8 | 1 |
GO:0030135 | coated vesicle | 7 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HSM9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007029 | endoplasmic reticulum organization | 5 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005537 | mannose binding | 4 | 1 |
GO:0030246 | carbohydrate binding | 2 | 2 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0048029 | monosaccharide binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.514 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.608 |
CLV_PCSK_FUR_1 | 441 | 445 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 385 | 387 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.704 |
CLV_PCSK_PC7_1 | 218 | 224 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.659 |
CLV_Separin_Metazoa | 403 | 407 | PF03568 | 0.410 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.551 |
DOC_CYCLIN_RxL_1 | 224 | 237 | PF00134 | 0.488 |
DOC_MAPK_gen_1 | 244 | 253 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 368 | 378 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 455 | 463 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 498 | 504 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 244 | 253 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 371 | 378 | PF00069 | 0.309 |
DOC_PP1_RVXF_1 | 113 | 119 | PF00149 | 0.256 |
DOC_PP1_RVXF_1 | 384 | 391 | PF00149 | 0.386 |
DOC_PP1_RVXF_1 | 499 | 505 | PF00149 | 0.448 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.367 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.269 |
DOC_SPAK_OSR1_1 | 117 | 121 | PF12202 | 0.269 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.423 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.342 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 329 | 333 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 444 | 450 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.282 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.606 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 110 | 118 | PF00928 | 0.363 |
LIG_deltaCOP1_diTrp_1 | 176 | 184 | PF00928 | 0.489 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.300 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.367 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.315 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.410 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.360 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.435 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.528 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.300 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.537 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.419 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.361 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.395 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.399 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.370 |
LIG_LIR_Apic_2 | 56 | 62 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 291 | 300 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 457 | 466 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 457 | 461 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.294 |
LIG_PDZ_Class_3 | 512 | 517 | PF00595 | 0.525 |
LIG_Pex14_2 | 229 | 233 | PF04695 | 0.490 |
LIG_Pex14_2 | 256 | 260 | PF04695 | 0.359 |
LIG_PTB_Apo_2 | 81 | 88 | PF02174 | 0.282 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.435 |
LIG_SH2_STAT3 | 145 | 148 | PF00017 | 0.282 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.354 |
LIG_SH3_1 | 506 | 512 | PF00018 | 0.458 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.507 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 360 | 367 | PF11976 | 0.311 |
LIG_SUMO_SIM_anti_2 | 399 | 407 | PF11976 | 0.411 |
LIG_SxIP_EBH_1 | 3 | 16 | PF03271 | 0.423 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.474 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.389 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.425 |
LIG_UBA3_1 | 228 | 234 | PF00899 | 0.614 |
MOD_CDK_SPxxK_3 | 162 | 169 | PF00069 | 0.663 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.353 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.575 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.423 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.655 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.503 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.501 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.488 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.437 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.657 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.384 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.325 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.680 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.498 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.584 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.595 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.423 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.420 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.547 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.436 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.394 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.366 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.503 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.643 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.450 |
MOD_NEK2_2 | 445 | 450 | PF00069 | 0.610 |
MOD_PK_1 | 235 | 241 | PF00069 | 0.539 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.644 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.444 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.304 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.620 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.404 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.499 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.264 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.323 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.523 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.323 |
MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.665 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.375 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.478 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.550 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.373 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.452 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.664 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.408 |
MOD_SUMO_for_1 | 384 | 387 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 448 | 458 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 473 | 481 | PF00179 | 0.407 |
TRG_DiLeu_BaEn_1 | 361 | 366 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 441 | 444 | PF00400 | 0.647 |
TRG_NES_CRM1_1 | 465 | 477 | PF08389 | 0.563 |
TRG_NLS_MonoCore_2 | 220 | 225 | PF00514 | 0.612 |
TRG_NLS_MonoCore_2 | 440 | 445 | PF00514 | 0.594 |
TRG_NLS_MonoExtC_3 | 220 | 225 | PF00514 | 0.612 |
TRG_NLS_MonoExtC_3 | 440 | 445 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 218 | 225 | PF00514 | 0.621 |
TRG_NLS_MonoExtN_4 | 439 | 446 | PF00514 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 472 | 477 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIA0 | Leptomonas seymouri | 78% | 100% |
A0A1X0NKB0 | Trypanosomatidae | 42% | 80% |
A0A3R7LT82 | Trypanosoma rangeli | 47% | 95% |
A0A3S5H5L7 | Leishmania donovani | 100% | 86% |
A4H4F2 | Leishmania braziliensis | 87% | 100% |
C9ZU67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 83% |
E8NHN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AKL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QJ95 | Leishmania major | 96% | 100% |
V5ARI9 | Trypanosoma cruzi | 46% | 88% |