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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HG16
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.496 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 337 | 339 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.380 |
DEG_APCC_DBOX_1 | 358 | 366 | PF00400 | 0.374 |
DOC_PP4_FxxP_1 | 151 | 154 | PF00568 | 0.478 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.528 |
DOC_USP7_UBL2_3 | 107 | 111 | PF12436 | 0.562 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.547 |
DOC_USP7_UBL2_3 | 222 | 226 | PF12436 | 0.569 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.409 |
LIG_14-3-3_CanoR_1 | 330 | 339 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 369 | 376 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 77 | 87 | PF00244 | 0.541 |
LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.527 |
LIG_EH1_1 | 269 | 277 | PF00400 | 0.521 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.533 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.392 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.552 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.479 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.419 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.643 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.558 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.381 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.374 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.349 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.501 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 266 | 276 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.406 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.488 |
LIG_PCNA_yPIPBox_3 | 283 | 293 | PF02747 | 0.546 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 268 | 272 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 323 | 327 | PF00017 | 0.543 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.558 |
LIG_SH3_4 | 222 | 229 | PF00018 | 0.329 |
LIG_SUMO_SIM_par_1 | 5 | 10 | PF11976 | 0.487 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.312 |
LIG_UBA3_1 | 134 | 143 | PF00899 | 0.430 |
LIG_UBA3_1 | 313 | 320 | PF00899 | 0.434 |
LIG_UBA3_1 | 361 | 367 | PF00899 | 0.535 |
LIG_WRC_WIRS_1 | 98 | 103 | PF05994 | 0.521 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.474 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.414 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.586 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.596 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.476 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.396 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.382 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.516 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.673 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.482 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.426 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.529 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.425 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.484 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.461 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.516 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.509 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.531 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.414 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.458 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.462 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.225 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.570 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.610 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.429 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.480 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.462 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.574 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.481 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.609 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.447 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.415 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.487 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.409 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.406 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.546 |
MOD_SUMO_rev_2 | 220 | 227 | PF00179 | 0.528 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.385 |
TRG_NLS_MonoExtN_4 | 364 | 370 | PF00514 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 359 | 363 | PF00026 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1A8 | Leptomonas seymouri | 64% | 100% |
A0A0S4J8X0 | Bodo saltans | 31% | 100% |
A0A1X0NG17 | Trypanosomatidae | 36% | 99% |
A0A3S7X117 | Leishmania donovani | 83% | 100% |
A0A422NDW9 | Trypanosoma rangeli | 36% | 99% |
A4I338 | Leishmania infantum | 83% | 100% |
C9ZJL0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 99% |
E9ACV6 | Leishmania major | 84% | 100% |
E9AZE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
V5BB08 | Trypanosoma cruzi | 36% | 99% |