A conserved but unique Kinetoplastid protein with 2-8 TM segments
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9B5Y7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 396 | 400 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 118 | 122 | PF00082 | 0.429 |
CLV_PCSK_FUR_1 | 300 | 304 | PF00082 | 0.524 |
CLV_PCSK_FUR_1 | 305 | 309 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.393 |
CLV_PCSK_PC7_1 | 303 | 309 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.329 |
CLV_Separin_Metazoa | 351 | 355 | PF03568 | 0.360 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.542 |
DEG_SPOP_SBC_1 | 269 | 273 | PF00917 | 0.481 |
DEG_SPOP_SBC_1 | 431 | 435 | PF00917 | 0.394 |
DOC_CDC14_PxL_1 | 35 | 43 | PF14671 | 0.379 |
DOC_CYCLIN_yCln2_LP_2 | 364 | 370 | PF00134 | 0.422 |
DOC_MAPK_DCC_7 | 33 | 43 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 32 | 40 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 354 | 361 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 316 | 324 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.242 |
DOC_MAPK_RevD_3 | 209 | 224 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 103 | 109 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 123 | 130 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 171 | 177 | PF00149 | 0.412 |
DOC_PP1_RVXF_1 | 491 | 498 | PF00149 | 0.369 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.413 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.443 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.446 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 132 | 141 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 173 | 179 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 208 | 214 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 260 | 266 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 452 | 458 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.458 |
LIG_AP2alpha_2 | 140 | 142 | PF02296 | 0.358 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.298 |
LIG_BRCT_BRCA1_1 | 467 | 471 | PF00533 | 0.461 |
LIG_CaM_IQ_9 | 291 | 307 | PF13499 | 0.494 |
LIG_CSL_BTD_1 | 70 | 73 | PF09270 | 0.459 |
LIG_EVH1_1 | 167 | 171 | PF00568 | 0.510 |
LIG_EVH1_2 | 171 | 175 | PF00568 | 0.333 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.560 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.342 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.363 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.521 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.516 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.284 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.343 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.369 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.398 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.544 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.387 |
LIG_IRF3_LxIS_1 | 182 | 188 | PF10401 | 0.370 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 379 | 388 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 496 | 505 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 75 | 86 | PF02991 | 0.540 |
LIG_LIR_LC3C_4 | 109 | 114 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 496 | 501 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.543 |
LIG_NRBOX | 348 | 354 | PF00104 | 0.371 |
LIG_NRBOX | 360 | 366 | PF00104 | 0.411 |
LIG_PALB2_WD40_1 | 73 | 81 | PF16756 | 0.445 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 386 | 390 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 386 | 389 | PF00017 | 0.439 |
LIG_SH2_STAT3 | 484 | 487 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.253 |
LIG_SH3_2 | 168 | 173 | PF14604 | 0.493 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.465 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.538 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.240 |
LIG_SH3_CIN85_PxpxPR_1 | 168 | 173 | PF14604 | 0.493 |
LIG_SUMO_SIM_anti_2 | 428 | 435 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 148 | 153 | PF11976 | 0.578 |
LIG_SUMO_SIM_par_1 | 209 | 215 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 428 | 435 | PF11976 | 0.432 |
LIG_TRFH_1 | 44 | 48 | PF08558 | 0.350 |
LIG_TYR_ITIM | 328 | 333 | PF00017 | 0.406 |
LIG_WRC_WIRS_1 | 494 | 499 | PF05994 | 0.492 |
LIG_WW_3 | 170 | 174 | PF00397 | 0.473 |
MOD_CDK_SPK_2 | 154 | 159 | PF00069 | 0.375 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.505 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.555 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.367 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.649 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.564 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.499 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.436 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.449 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.629 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.397 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.593 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.396 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.789 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.679 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.430 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.497 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.462 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.450 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.440 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.602 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.606 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.622 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.681 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.678 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.453 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.384 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.429 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.430 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.648 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.479 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.500 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.443 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.424 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.455 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.365 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.341 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.363 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.365 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.404 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.403 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.393 |
MOD_NEK2_2 | 355 | 360 | PF00069 | 0.461 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.402 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.603 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.646 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.361 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.574 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.572 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.413 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.416 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.338 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.398 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.515 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.394 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.369 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.618 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.425 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.453 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.459 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.518 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.427 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.482 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.600 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.382 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 122 | 127 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 146 | 151 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.286 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 305 | 308 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 309 | 312 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.456 |
TRG_NLS_Bipartite_1 | 289 | 311 | PF00514 | 0.373 |
TRG_NLS_MonoCore_2 | 305 | 310 | PF00514 | 0.385 |
TRG_NLS_MonoExtC_3 | 119 | 124 | PF00514 | 0.449 |
TRG_NLS_MonoExtC_3 | 305 | 310 | PF00514 | 0.385 |
TRG_NLS_MonoExtN_4 | 118 | 124 | PF00514 | 0.456 |
TRG_NLS_MonoExtN_4 | 303 | 310 | PF00514 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 296 | 301 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JMW3 | Bodo saltans | 21% | 100% |
A0A3S5H7Y7 | Leishmania donovani | 90% | 100% |
A0A422N586 | Trypanosoma rangeli | 33% | 85% |
A4IB04 | Leishmania infantum | 90% | 100% |
C9ZNK4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 85% |
E9AET2 | Leishmania major | 89% | 100% |
V5D9L8 | Trypanosoma cruzi | 32% | 84% |