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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q929
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.491 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 165 | 169 | PF03568 | 0.467 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.652 |
DOC_CKS1_1 | 126 | 131 | PF01111 | 0.463 |
DOC_PP1_RVXF_1 | 107 | 113 | PF00149 | 0.393 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.410 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.536 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.686 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.540 |
LIG_Actin_WH2_2 | 103 | 120 | PF00022 | 0.494 |
LIG_Actin_WH2_2 | 180 | 196 | PF00022 | 0.522 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.453 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.530 |
LIG_Clathr_ClatBox_1 | 314 | 318 | PF01394 | 0.603 |
LIG_deltaCOP1_diTrp_1 | 250 | 256 | PF00928 | 0.459 |
LIG_EH1_1 | 293 | 301 | PF00400 | 0.461 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.464 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.538 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.460 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.418 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.511 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.518 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.467 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.559 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.601 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.210 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.487 |
LIG_LIR_Apic_2 | 98 | 103 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 105 | 114 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.514 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.385 |
LIG_PCNA_yPIPBox_3 | 302 | 315 | PF02747 | 0.561 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.382 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.398 |
LIG_Pex14_2 | 86 | 90 | PF04695 | 0.601 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.553 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.500 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.398 |
LIG_SH3_1 | 100 | 106 | PF00018 | 0.581 |
LIG_SH3_1 | 313 | 319 | PF00018 | 0.623 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.566 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.564 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.632 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.554 |
LIG_SH3_4 | 208 | 215 | PF00018 | 0.664 |
LIG_SH3_5 | 96 | 100 | PF00018 | 0.607 |
LIG_Sin3_3 | 11 | 18 | PF02671 | 0.432 |
LIG_SUMO_SIM_anti_2 | 10 | 16 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 295 | 301 | PF11976 | 0.432 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.609 |
LIG_UBA3_1 | 113 | 118 | PF00899 | 0.405 |
LIG_ULM_U2AF65_1 | 71 | 76 | PF00076 | 0.596 |
LIG_WRC_WIRS_1 | 83 | 88 | PF05994 | 0.645 |
MOD_CDK_SPxxK_3 | 102 | 109 | PF00069 | 0.524 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.464 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.614 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.524 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.358 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.568 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.519 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.460 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.572 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.475 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.493 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.502 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.520 |
MOD_GlcNHglycan | 22 | 26 | PF01048 | 0.449 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.482 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.413 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.728 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.512 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.476 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.517 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.584 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.202 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.590 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.536 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.361 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.523 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.558 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.440 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.515 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.595 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.514 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.538 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.512 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.490 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.553 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.489 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.602 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.525 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.664 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.453 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.398 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.635 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.507 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.455 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.467 |
MOD_SUMO_for_1 | 319 | 322 | PF00179 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 310 | 315 | PF01217 | 0.526 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.469 |
TRG_NES_CRM1_1 | 283 | 295 | PF08389 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 313 | 318 | PF00026 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAG5 | Leptomonas seymouri | 79% | 99% |
A0A0S4JUF0 | Bodo saltans | 36% | 99% |
A0A1X0NS29 | Trypanosomatidae | 45% | 100% |
A0A3R7KFL2 | Trypanosoma rangeli | 43% | 100% |
A0A3S7WZW5 | Leishmania donovani | 97% | 100% |
A4HF20 | Leishmania braziliensis | 89% | 100% |
A4I299 | Leishmania infantum | 96% | 100% |
E9AYE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5AKX8 | Trypanosoma cruzi | 47% | 99% |