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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HH43
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
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 | 283 | 287 | PF00656 | 0.673 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.585 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.739 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.577 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.595 |
DOC_CKS1_1 | 102 | 107 | PF01111 | 0.731 |
DOC_CYCLIN_RxL_1 | 305 | 313 | PF00134 | 0.605 |
DOC_CYCLIN_RxL_1 | 9 | 22 | PF00134 | 0.665 |
DOC_MAPK_gen_1 | 224 | 232 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 5 | 13 | PF00069 | 0.678 |
DOC_MAPK_gen_1 | 57 | 68 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 166 | 174 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 224 | 232 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.580 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.589 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.679 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.713 |
LIG_14-3-3_CanoR_1 | 281 | 291 | PF00244 | 0.696 |
LIG_AP2alpha_2 | 380 | 382 | PF02296 | 0.519 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.668 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.569 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.629 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.487 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.663 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.566 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.694 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.538 |
LIG_LIR_Apic_2 | 288 | 294 | PF02991 | 0.663 |
LIG_LIR_Gen_1 | 150 | 158 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 84 | 92 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.564 |
LIG_NRBOX | 387 | 393 | PF00104 | 0.655 |
LIG_Pex14_1 | 143 | 147 | PF04695 | 0.543 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.539 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.643 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.529 |
LIG_SH2_NCK_1 | 152 | 156 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 358 | 362 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.529 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.636 |
LIG_SH3_2 | 102 | 107 | PF14604 | 0.731 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.642 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.701 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.653 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.606 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.837 |
LIG_SH3_4 | 5 | 12 | PF00018 | 0.679 |
LIG_SUMO_SIM_anti_2 | 384 | 390 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 227 | 233 | PF11976 | 0.563 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.636 |
LIG_TYR_ITIM | 356 | 361 | PF00017 | 0.524 |
LIG_TYR_ITIM | 89 | 94 | PF00017 | 0.620 |
MOD_CDK_SPK_2 | 98 | 103 | PF00069 | 0.556 |
MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.728 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.562 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.643 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.596 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.531 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.532 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.622 |
MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.610 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.609 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.643 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.592 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.540 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.588 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.494 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.621 |
MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.611 |
MOD_GlcNHglycan | 397 | 401 | PF01048 | 0.627 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.640 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.642 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.683 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.746 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.635 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.538 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.632 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.541 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.600 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.450 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.622 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.645 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.585 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.677 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.620 |
MOD_PK_1 | 224 | 230 | PF00069 | 0.422 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.696 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.698 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.521 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.638 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.696 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.699 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.602 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.660 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.559 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.645 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.654 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.714 |
MOD_SUMO_for_1 | 190 | 193 | PF00179 | 0.715 |
MOD_SUMO_rev_2 | 163 | 168 | PF00179 | 0.741 |
MOD_SUMO_rev_2 | 186 | 192 | PF00179 | 0.608 |
TRG_DiLeu_BaEn_4 | 279 | 285 | PF01217 | 0.666 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.636 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X275 | Leishmania donovani | 68% | 100% |
A4I496 | Leishmania infantum | 68% | 100% |
E9ADP3 | Leishmania major | 69% | 98% |
E9AM37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |