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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HGJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.757 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.591 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.767 |
DOC_CDC14_PxL_1 | 38 | 46 | PF14671 | 0.508 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.663 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.671 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.643 |
DOC_MAPK_DCC_7 | 183 | 191 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 20 | 27 | PF00069 | 0.558 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.582 |
DOC_PP2B_LxvP_1 | 269 | 272 | PF13499 | 0.809 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.693 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.735 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.830 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 220 | 228 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 91 | 99 | PF00244 | 0.522 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.793 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.781 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.595 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.746 |
LIG_IBAR_NPY_1 | 369 | 371 | PF08397 | 0.805 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 203 | 208 | PF02991 | 0.702 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.561 |
LIG_MLH1_MIPbox_1 | 221 | 225 | PF16413 | 0.523 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.501 |
LIG_PTB_Apo_2 | 158 | 165 | PF02174 | 0.481 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.550 |
LIG_SH2_SRC | 371 | 374 | PF00017 | 0.811 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.814 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.663 |
LIG_SH3_1 | 333 | 339 | PF00018 | 0.659 |
LIG_SH3_2 | 385 | 390 | PF14604 | 0.798 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.641 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.654 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.714 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.659 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.752 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.544 |
MOD_CDC14_SPxK_1 | 387 | 390 | PF00782 | 0.636 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.609 |
MOD_CDK_SPK_2 | 182 | 187 | PF00069 | 0.734 |
MOD_CDK_SPK_2 | 356 | 361 | PF00069 | 0.830 |
MOD_CDK_SPxK_1 | 136 | 142 | PF00069 | 0.763 |
MOD_CDK_SPxK_1 | 384 | 390 | PF00069 | 0.629 |
MOD_CDK_SPxxK_3 | 142 | 149 | PF00069 | 0.671 |
MOD_CDK_SPxxK_3 | 19 | 26 | PF00069 | 0.656 |
MOD_CDK_SPxxK_3 | 384 | 391 | PF00069 | 0.660 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.599 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.712 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.718 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.781 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.769 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.757 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.696 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.822 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.710 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.609 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.760 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.621 |
MOD_Cter_Amidation | 106 | 109 | PF01082 | 0.576 |
MOD_DYRK1A_RPxSP_1 | 142 | 146 | PF00069 | 0.698 |
MOD_DYRK1A_RPxSP_1 | 149 | 153 | PF00069 | 0.596 |
MOD_DYRK1A_RPxSP_1 | 300 | 304 | PF00069 | 0.802 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.737 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.795 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.735 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.494 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.688 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.838 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.541 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.542 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.737 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.531 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.655 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.674 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.672 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.669 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.600 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.586 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.729 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.672 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.667 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.608 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.697 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.630 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.685 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.265 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.760 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.650 |
MOD_N-GLC_2 | 110 | 112 | PF02516 | 0.411 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.438 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.527 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.793 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.530 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.574 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.813 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.562 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.669 |
MOD_OFUCOSY | 120 | 126 | PF10250 | 0.346 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.514 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.551 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.546 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.664 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.577 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.551 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.745 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.546 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.661 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.645 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.664 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.775 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.692 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.698 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.586 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.650 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.527 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.701 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.761 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.829 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.563 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.579 |
TRG_DiLeu_BaEn_1 | 293 | 298 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7W6 | Leptomonas seymouri | 38% | 100% |
A0A3S7X1G7 | Leishmania donovani | 69% | 100% |
E9ADK0 | Leishmania major | 68% | 100% |
E9AHG4 | Leishmania infantum | 69% | 100% |
E9AZW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |