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. | yes | yes: 20 |
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 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AU51
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050657 | nucleic acid transport | 6 | 1 |
GO:0050658 | RNA transport | 4 | 1 |
GO:0051028 | mRNA transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051236 | establishment of RNA localization | 3 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.789 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.662 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.767 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.595 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.726 |
DOC_CYCLIN_RxL_1 | 265 | 274 | PF00134 | 0.647 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.712 |
DOC_MAPK_MEF2A_6 | 243 | 251 | PF00069 | 0.442 |
DOC_PP4_FxxP_1 | 18 | 21 | PF00568 | 0.805 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.579 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.603 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 275 | 279 | PF12436 | 0.560 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.841 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.739 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.541 |
LIG_BIR_III_4 | 188 | 192 | PF00653 | 0.750 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.763 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.824 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.665 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.633 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.553 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.770 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.669 |
LIG_LIR_Apic_2 | 17 | 21 | PF02991 | 0.803 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.753 |
LIG_MLH1_MIPbox_1 | 28 | 32 | PF16413 | 0.558 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.784 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.563 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.718 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.808 |
LIG_SUMO_SIM_par_1 | 281 | 289 | PF11976 | 0.572 |
LIG_UBA3_1 | 270 | 275 | PF00899 | 0.644 |
LIG_WRC_WIRS_1 | 153 | 158 | PF05994 | 0.692 |
MOD_CDK_SPK_2 | 57 | 62 | PF00069 | 0.698 |
MOD_CDK_SPxK_1 | 105 | 111 | PF00069 | 0.561 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.713 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.797 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.792 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.771 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.764 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.541 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.715 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.691 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.700 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.646 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.668 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.696 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.569 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.825 |
MOD_GlcNHglycan | 200 | 204 | PF01048 | 0.742 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.678 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.643 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.698 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.669 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.633 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.721 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.753 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.557 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.564 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.630 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.710 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.698 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.731 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.552 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.564 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.545 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.515 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.464 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.571 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.777 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.818 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.601 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.687 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.561 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.567 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.689 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.550 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.510 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.844 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.713 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.608 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.739 |
MOD_SUMO_rev_2 | 172 | 182 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 230 | 239 | PF00179 | 0.661 |
MOD_SUMO_rev_2 | 241 | 245 | PF00179 | 0.642 |
MOD_SUMO_rev_2 | 274 | 281 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_1 | 277 | 282 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 250 | 255 | PF01217 | 0.545 |
TRG_NLS_MonoExtC_3 | 159 | 165 | PF00514 | 0.782 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFC6 | Leptomonas seymouri | 55% | 77% |
A0A0S4IHX6 | Bodo saltans | 28% | 92% |
A0A3Q8IWI8 | Leishmania donovani | 89% | 100% |
A4HQD5 | Leishmania braziliensis | 69% | 100% |
A4IE27 | Leishmania infantum | 89% | 100% |
Q4Q0E4 | Leishmania major | 89% | 99% |