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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 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 |
Related structures:
AlphaFold database: A0A3S7X6H7
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 8 |
GO:0005488 | binding | 1 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.598 |
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.605 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.813 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.603 |
CLV_PCSK_FUR_1 | 30 | 34 | PF00082 | 0.568 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.813 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.505 |
CLV_PCSK_PC7_1 | 31 | 37 | PF00082 | 0.508 |
CLV_Separin_Metazoa | 139 | 143 | PF03568 | 0.709 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.579 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.471 |
DOC_PP1_RVXF_1 | 206 | 213 | PF00149 | 0.690 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.567 |
DOC_USP7_UBL2_3 | 166 | 170 | PF12436 | 0.600 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.698 |
LIG_CaM_IQ_9 | 346 | 362 | PF13499 | 0.363 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.671 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.548 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.664 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.622 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.661 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.171 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.545 |
LIG_Pex14_1 | 22 | 26 | PF04695 | 0.511 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.303 |
LIG_PTAP_UEV_1 | 156 | 161 | PF05743 | 0.489 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.502 |
LIG_SH3_1 | 249 | 255 | PF00018 | 0.544 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.727 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.598 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.561 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.383 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.538 |
LIG_WW_3 | 139 | 143 | PF00397 | 0.709 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.554 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.727 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.541 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.509 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.363 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.662 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.699 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.751 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.550 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.171 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.712 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.611 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.620 |
MOD_Cter_Amidation | 205 | 208 | PF01082 | 0.714 |
MOD_Cter_Amidation | 374 | 377 | PF01082 | 0.429 |
MOD_GlcNHglycan | 102 | 106 | PF01048 | 0.583 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.584 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.637 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.673 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.567 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.566 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.729 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.303 |
MOD_GlcNHglycan | 49 | 54 | PF01048 | 0.643 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.477 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.581 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.665 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.599 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.683 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.680 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.489 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.674 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.363 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.697 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.746 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.554 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.514 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.303 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.489 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.682 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.508 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.303 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.620 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.669 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.680 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.444 |
MOD_Plk_2-3 | 43 | 49 | PF00069 | 0.611 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.700 |
TRG_DiLeu_BaEn_2 | 367 | 373 | PF01217 | 0.333 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.547 |
TRG_ER_diLys_1 | 376 | 379 | PF00400 | 0.535 |
TRG_NLS_Bipartite_1 | 192 | 211 | PF00514 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.303 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC1 | Leptomonas seymouri | 50% | 91% |
A0A422N868 | Trypanosoma rangeli | 34% | 100% |
A4HL96 | Leishmania braziliensis | 76% | 99% |
A4I8S2 | Leishmania infantum | 100% | 100% |
E9B3N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q4E9 | Leishmania major | 91% | 100% |