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 |
Related structures:
AlphaFold database: A4H5V1
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0008270 | zinc ion binding | 6 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
GO:0046914 | transition metal ion binding | 5 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.503 |
CLV_PCSK_FUR_1 | 77 | 81 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.596 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.566 |
DOC_CDC14_PxL_1 | 197 | 205 | PF14671 | 0.566 |
DOC_CDC14_PxL_1 | 301 | 309 | PF14671 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 203 | 209 | PF00134 | 0.572 |
DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 153 | 161 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 190 | 199 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 262 | 271 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 80 | 89 | PF00069 | 0.523 |
DOC_PP2B_LxvP_1 | 60 | 63 | PF13499 | 0.619 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.439 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.506 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.375 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 293 | 301 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.651 |
LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.497 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.533 |
LIG_EVH1_1 | 200 | 204 | PF00568 | 0.552 |
LIG_EVH1_1 | 301 | 305 | PF00568 | 0.436 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.498 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.432 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.576 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.513 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.468 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.506 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.410 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.487 |
LIG_LIR_Apic_2 | 164 | 169 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 149 | 159 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 265 | 276 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 321 | 329 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 321 | 325 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.495 |
LIG_LYPXL_yS_3 | 304 | 307 | PF13949 | 0.614 |
LIG_Pex14_1 | 218 | 222 | PF04695 | 0.442 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.508 |
LIG_Pex14_2 | 95 | 99 | PF04695 | 0.447 |
LIG_PTAP_UEV_1 | 340 | 345 | PF05743 | 0.557 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.470 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.597 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.398 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.511 |
LIG_SH2_STAT3 | 316 | 319 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.427 |
LIG_SH3_1 | 338 | 344 | PF00018 | 0.560 |
LIG_SH3_2 | 305 | 310 | PF14604 | 0.528 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.494 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.626 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.559 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.435 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.426 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.560 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.478 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.626 |
LIG_TYR_ITIM | 89 | 94 | PF00017 | 0.346 |
LIG_TYR_ITSM | 147 | 154 | PF00017 | 0.337 |
LIG_UBA3_1 | 279 | 288 | PF00899 | 0.511 |
LIG_WW_2 | 201 | 204 | PF00397 | 0.549 |
LIG_WW_2 | 305 | 308 | PF00397 | 0.446 |
LIG_WW_3 | 38 | 42 | PF00397 | 0.453 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.461 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.457 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.380 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.549 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.505 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.412 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.547 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.617 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.549 |
MOD_Cter_Amidation | 77 | 80 | PF01082 | 0.529 |
MOD_DYRK1A_RPxSP_1 | 8 | 12 | PF00069 | 0.512 |
MOD_GlcNHglycan | 106 | 112 | PF01048 | 0.432 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.490 |
MOD_GlcNHglycan | 253 | 257 | PF01048 | 0.594 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.617 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.725 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.602 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.427 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.487 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.634 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.526 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.488 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.506 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.472 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.547 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.586 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.483 |
MOD_N-GLC_2 | 242 | 244 | PF02516 | 0.454 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.588 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.506 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.442 |
MOD_PK_1 | 363 | 369 | PF00069 | 0.463 |
MOD_PKA_1 | 284 | 290 | PF00069 | 0.398 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.583 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.398 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.409 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.564 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.687 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.385 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.561 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.549 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.616 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.554 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.681 |
MOD_SUMO_for_1 | 362 | 365 | PF00179 | 0.663 |
TRG_DiLeu_BaEn_2 | 29 | 35 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_2 | 317 | 323 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P570 | Leptomonas seymouri | 43% | 100% |
A0A0S4JNP6 | Bodo saltans | 24% | 100% |
A0A3S7WQU3 | Leishmania donovani | 65% | 100% |
A4HU45 | Leishmania infantum | 65% | 100% |
E9AMX4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4QHQ2 | Leishmania major | 65% | 99% |
V5DEB3 | Trypanosoma cruzi | 25% | 100% |