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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0140513 | nuclear protein-containing complex | 2 | 8 |
GO:0044613 | nuclear pore central transport channel | 3 | 1 |
Related structures:
AlphaFold database: E9B289
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 1 |
GO:0006607 | NLS-bearing protein import into nucleus | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0006997 | nucleus organization | 5 | 1 |
GO:0006999 | nuclear pore organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034504 | protein localization to nucleus | 6 | 1 |
GO:0036228 | protein localization to nuclear inner membrane | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051170 | import into nucleus | 6 | 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:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090435 | protein localization to nuclear envelope | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 1 |
GO:0017056 | structural constituent of nuclear pore | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.302 |
CLV_Separin_Metazoa | 247 | 251 | PF03568 | 0.307 |
CLV_Separin_Metazoa | 309 | 313 | PF03568 | 0.355 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.735 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.522 |
DOC_MAPK_gen_1 | 250 | 261 | PF00069 | 0.352 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.338 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.711 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.662 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.639 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.307 |
DOC_USP7_UBL2_3 | 429 | 433 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 164 | 172 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 313 | 323 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 349 | 359 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 390 | 398 | PF00244 | 0.450 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_2 | 14 | 20 | PF00533 | 0.465 |
LIG_Clathr_ClatBox_1 | 172 | 176 | PF01394 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 409 | 413 | PF00928 | 0.411 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.588 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.486 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.641 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.307 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.581 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.425 |
LIG_LIR_Apic_2 | 111 | 116 | PF02991 | 0.635 |
LIG_LIR_Apic_2 | 57 | 62 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 176 | 184 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 409 | 417 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 409 | 413 | PF02991 | 0.426 |
LIG_NRBOX | 330 | 336 | PF00104 | 0.460 |
LIG_NRBOX | 423 | 429 | PF00104 | 0.455 |
LIG_PCNA_PIPBox_1 | 165 | 174 | PF02747 | 0.401 |
LIG_PCNA_yPIPBox_3 | 164 | 172 | PF02747 | 0.474 |
LIG_PCNA_yPIPBox_3 | 256 | 270 | PF02747 | 0.307 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.648 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.388 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.338 |
LIG_SH2_GRB2like | 213 | 216 | PF00017 | 0.504 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.363 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.702 |
LIG_SUMO_SIM_par_1 | 155 | 161 | PF11976 | 0.665 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.609 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.615 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.768 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.355 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.262 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.429 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.352 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.653 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.618 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.499 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.576 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.593 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.649 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.561 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.590 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.686 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.603 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.505 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.675 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.492 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.510 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.620 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.645 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.401 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.411 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.665 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.618 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.739 |
MOD_N-GLC_1 | 367 | 372 | PF02516 | 0.555 |
MOD_N-GLC_2 | 194 | 196 | PF02516 | 0.360 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.592 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.482 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.575 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.641 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.355 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.455 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.561 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.598 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.385 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.508 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.318 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.486 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.480 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.355 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.456 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.458 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.487 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.466 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.462 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.297 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.329 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.639 |
MOD_SUMO_rev_2 | 426 | 435 | PF00179 | 0.464 |
TRG_DiLeu_BaEn_2 | 346 | 352 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 438 | 441 | PF00400 | 0.471 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JWT3 | Bodo saltans | 33% | 95% |
A0A3Q8ICT1 | Leishmania donovani | 88% | 99% |
A0A3R7KYW1 | Trypanosoma rangeli | 40% | 100% |
A4HJS8 | Leishmania braziliensis | 75% | 100% |
A4I794 | Leishmania infantum | 86% | 99% |
O42963 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
P48837 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 82% |
Q4Q5W9 | Leishmania major | 80% | 99% |