Nuclear proteins, nuclear transmembrane 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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031965 | nuclear membrane | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4IAY1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.626 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.531 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.525 |
DEG_SPOP_SBC_1 | 330 | 334 | PF00917 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 276 | 282 | PF00134 | 0.411 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.266 |
DOC_PP2B_LxvP_1 | 202 | 205 | PF13499 | 0.721 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.474 |
DOC_PP2B_LxvP_1 | 275 | 278 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 60 | 63 | PF13499 | 0.665 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.708 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.659 |
DOC_USP7_UBL2_3 | 400 | 404 | PF12436 | 0.266 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.781 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 156 | 163 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 328 | 335 | PF00244 | 0.540 |
LIG_Actin_WH2_2 | 305 | 320 | PF00022 | 0.355 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.694 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.714 |
LIG_Clathr_ClatBox_1 | 390 | 394 | PF01394 | 0.513 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.751 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.465 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.494 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.464 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.411 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.771 |
LIG_GBD_Chelix_1 | 309 | 317 | PF00786 | 0.697 |
LIG_GBD_Chelix_1 | 385 | 393 | PF00786 | 0.402 |
LIG_LIR_Apic_2 | 229 | 235 | PF02991 | 0.709 |
LIG_LIR_Apic_2 | 80 | 86 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.695 |
LIG_LIR_Gen_1 | 266 | 276 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 356 | 364 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 387 | 396 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 356 | 360 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 387 | 391 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 95 | 99 | PF02991 | 0.721 |
LIG_NRBOX | 270 | 276 | PF00104 | 0.299 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.474 |
LIG_REV1ctd_RIR_1 | 9 | 18 | PF16727 | 0.474 |
LIG_RPA_C_Fungi | 334 | 346 | PF08784 | 0.479 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.718 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.555 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 19 | 23 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.625 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.474 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.812 |
LIG_SUMO_SIM_anti_2 | 356 | 362 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 382 | 387 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 387 | 395 | PF11976 | 0.416 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.760 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.630 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.618 |
LIG_TRFH_1 | 33 | 37 | PF08558 | 0.625 |
LIG_WRC_WIRS_1 | 385 | 390 | PF05994 | 0.513 |
MOD_CDK_SPxK_1 | 68 | 74 | PF00069 | 0.633 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.685 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.808 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.732 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.623 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.465 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.698 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.733 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.643 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.631 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.599 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.622 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.411 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.634 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.727 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.742 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.645 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.720 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.622 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.651 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.620 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.600 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.671 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.655 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.702 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.579 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.633 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.643 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.612 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.697 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.433 |
MOD_OFUCOSY | 365 | 371 | PF10250 | 0.411 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.701 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.641 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.660 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.723 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.619 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.691 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.481 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.411 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.674 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.609 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.641 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.565 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.587 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.493 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.513 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.700 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.701 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.776 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.639 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.639 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.740 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.658 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 316 | 319 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHG2 | Leptomonas seymouri | 45% | 99% |
A0A3Q8IP51 | Leishmania donovani | 99% | 100% |
A4HMB5 | Leishmania braziliensis | 70% | 96% |
E9AEQ9 | Leishmania major | 89% | 100% |
E9B5W4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |