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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HVV3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.448 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.409 |
CLV_PCSK_FUR_1 | 303 | 307 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.383 |
CLV_PCSK_PC7_1 | 223 | 229 | PF00082 | 0.409 |
CLV_PCSK_PC7_1 | 394 | 400 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.291 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.595 |
DEG_APCC_DBOX_1 | 227 | 235 | PF00400 | 0.583 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.622 |
DEG_Kelch_Keap1_1 | 509 | 514 | PF01344 | 0.654 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.708 |
DEG_SCF_TRCP1_1 | 511 | 516 | PF00400 | 0.689 |
DOC_MAPK_FxFP_2 | 151 | 154 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 223 | 231 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 303 | 309 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 465 | 473 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.522 |
DOC_MAPK_JIP1_4 | 263 | 269 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 293 | 301 | PF00069 | 0.537 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 151 | 154 | PF00568 | 0.506 |
DOC_USP7_UBL2_3 | 461 | 465 | PF12436 | 0.544 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 132 | 138 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 432 | 440 | PF00244 | 0.659 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.443 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.697 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.512 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.605 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.670 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.530 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.446 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.580 |
LIG_LIR_Apic_2 | 106 | 111 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 165 | 171 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 190 | 198 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 496 | 501 | PF02991 | 0.474 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.508 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.536 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.552 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.513 |
LIG_Pex14_2 | 35 | 39 | PF04695 | 0.697 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.451 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.575 |
LIG_SH2_SRC | 7 | 10 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.609 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.498 |
LIG_SUMO_SIM_anti_2 | 170 | 176 | PF11976 | 0.554 |
LIG_SUMO_SIM_anti_2 | 216 | 222 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 170 | 176 | PF11976 | 0.511 |
LIG_SxIP_EBH_1 | 204 | 214 | PF03271 | 0.488 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.594 |
LIG_UBA3_1 | 448 | 454 | PF00899 | 0.488 |
LIG_WRC_WIRS_1 | 18 | 23 | PF05994 | 0.738 |
MOD_CDC14_SPxK_1 | 30 | 33 | PF00782 | 0.620 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.727 |
MOD_CDK_SPxxK_3 | 27 | 34 | PF00069 | 0.624 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.491 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.698 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.549 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.676 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.765 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.531 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.523 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.581 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.729 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.606 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.569 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.575 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.325 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.275 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.576 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.435 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.378 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.275 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.426 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.457 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.488 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.697 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.503 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.705 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.567 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.534 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.764 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.652 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.477 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.340 |
MOD_N-GLC_2 | 91 | 93 | PF02516 | 0.391 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.503 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.619 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.474 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.532 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.505 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.565 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.533 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.491 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.452 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.506 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.567 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.736 |
MOD_PK_1 | 13 | 19 | PF00069 | 0.726 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.582 |
MOD_PKA_1 | 33 | 39 | PF00069 | 0.583 |
MOD_PKA_1 | 432 | 438 | PF00069 | 0.647 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.652 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.506 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.681 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.636 |
MOD_PKB_1 | 11 | 19 | PF00069 | 0.637 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.555 |
MOD_Plk_2-3 | 101 | 107 | PF00069 | 0.494 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.631 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.478 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.567 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.508 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.552 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.322 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.744 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.603 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.703 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.550 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.570 |
MOD_SUMO_for_1 | 411 | 414 | PF00179 | 0.561 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.669 |
TRG_NES_CRM1_1 | 363 | 375 | PF08389 | 0.509 |
TRG_NES_CRM1_1 | 462 | 477 | PF08389 | 0.540 |
TRG_NLS_MonoExtN_4 | 303 | 308 | PF00514 | 0.629 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6B2 | Leptomonas seymouri | 24% | 100% |
A0A0N1IK13 | Leptomonas seymouri | 79% | 99% |
A0A0S4ITI3 | Bodo saltans | 44% | 100% |
A0A1X0NQB1 | Trypanosomatidae | 57% | 100% |
A0A1X0NVK2 | Trypanosomatidae | 23% | 100% |
A0A3S7WSV3 | Leishmania donovani | 100% | 100% |
A0A3S7WYG6 | Leishmania donovani | 26% | 100% |
A0A422N8L2 | Trypanosoma rangeli | 23% | 100% |
A4H7H2 | Leishmania braziliensis | 86% | 100% |
A4HDG4 | Leishmania braziliensis | 26% | 100% |
C9ZT74 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
D0A774 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9APK5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AWU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4QAM5 | Leishmania major | 25% | 100% |
Q4QFX4 | Leishmania major | 97% | 100% |
V5BD52 | Trypanosoma cruzi | 57% | 100% |
V5DSF1 | Trypanosoma cruzi | 22% | 100% |