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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005643 | nuclear pore | 3 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H7K5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.658 |
CLV_PCSK_FUR_1 | 190 | 194 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.625 |
CLV_PCSK_PC7_1 | 197 | 203 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.771 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.447 |
DEG_SCF_FBW7_2 | 81 | 87 | PF00400 | 0.686 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.619 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.607 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.620 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.572 |
DOC_USP7_UBL2_3 | 149 | 153 | PF12436 | 0.559 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.541 |
DOC_USP7_UBL2_3 | 182 | 186 | PF12436 | 0.619 |
DOC_USP7_UBL2_3 | 222 | 226 | PF12436 | 0.462 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 202 | 208 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 70 | 88 | PF00022 | 0.468 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.608 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.442 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.483 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.452 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.481 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.617 |
LIG_SH3_4 | 182 | 189 | PF00018 | 0.577 |
MOD_CDC14_SPxK_1 | 114 | 117 | PF00782 | 0.656 |
MOD_CDC14_SPxK_1 | 118 | 121 | PF00782 | 0.651 |
MOD_CDC14_SPxK_1 | 141 | 144 | PF00782 | 0.636 |
MOD_CDC14_SPxK_1 | 151 | 154 | PF00782 | 0.574 |
MOD_CDC14_SPxK_1 | 161 | 164 | PF00782 | 0.629 |
MOD_CDC14_SPxK_1 | 169 | 172 | PF00782 | 0.589 |
MOD_CDC14_SPxK_1 | 177 | 180 | PF00782 | 0.512 |
MOD_CDC14_SPxK_1 | 96 | 99 | PF00782 | 0.641 |
MOD_CDK_SPK_2 | 133 | 138 | PF00069 | 0.601 |
MOD_CDK_SPK_2 | 148 | 153 | PF00069 | 0.550 |
MOD_CDK_SPK_2 | 158 | 163 | PF00069 | 0.719 |
MOD_CDK_SPK_2 | 210 | 215 | PF00069 | 0.480 |
MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.649 |
MOD_CDK_SPxK_1 | 133 | 139 | PF00069 | 0.574 |
MOD_CDK_SPxK_1 | 148 | 154 | PF00069 | 0.513 |
MOD_CDK_SPxK_1 | 158 | 164 | PF00069 | 0.642 |
MOD_CDK_SPxK_1 | 166 | 172 | PF00069 | 0.577 |
MOD_CDK_SPxK_1 | 174 | 180 | PF00069 | 0.530 |
MOD_CDK_SPxK_1 | 80 | 86 | PF00069 | 0.755 |
MOD_CDK_SPxK_1 | 93 | 99 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 208 | 215 | PF00069 | 0.561 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.640 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.671 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.671 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.628 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.486 |
MOD_DYRK1A_RPxSP_1 | 121 | 125 | PF00069 | 0.732 |
MOD_DYRK1A_RPxSP_1 | 172 | 176 | PF00069 | 0.691 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.624 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.625 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.370 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.617 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.620 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.652 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.632 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.650 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.668 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.586 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.459 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.569 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.593 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.529 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.678 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.493 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.560 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.640 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.713 |
MOD_PK_1 | 226 | 232 | PF00069 | 0.517 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.733 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.692 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.589 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.533 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.643 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.606 |
MOD_PKB_1 | 191 | 199 | PF00069 | 0.586 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.544 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.545 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.597 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.591 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.620 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.543 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.536 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.642 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.577 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.530 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.474 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.555 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.734 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.616 |
MOD_SUMO_rev_2 | 87 | 93 | PF00179 | 0.584 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAS3 | Leptomonas seymouri | 53% | 97% |
A0A1X0NZQ5 | Trypanosomatidae | 33% | 77% |
A4HH60 | Leishmania braziliensis | 74% | 100% |
C9ZKP8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 80% |
E9ADM9 | Leishmania major | 93% | 100% |
E9AM51 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 97% |
V5DLD7 | Trypanosoma cruzi | 35% | 94% |