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 |
Related structures:
AlphaFold database: A4IE11
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 130 | 134 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.492 |
CLV_PCSK_FUR_1 | 248 | 252 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 225 | 227 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.452 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.420 |
DEG_SPOP_SBC_1 | 340 | 344 | PF00917 | 0.644 |
DOC_CDC14_PxL_1 | 50 | 58 | PF14671 | 0.422 |
DOC_CYCLIN_RxL_1 | 35 | 43 | PF00134 | 0.457 |
DOC_CYCLIN_yCln2_LP_2 | 217 | 220 | PF00134 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 256 | 262 | PF00134 | 0.432 |
DOC_MAPK_DCC_7 | 215 | 223 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 248 | 257 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 85 | 94 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 215 | 223 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 4 | 11 | PF00069 | 0.461 |
DOC_MAPK_NFAT4_5 | 4 | 12 | PF00069 | 0.486 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.473 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.560 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.525 |
LIG_deltaCOP1_diTrp_1 | 59 | 67 | PF00928 | 0.442 |
LIG_EVH1_1 | 387 | 391 | PF00568 | 0.434 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.427 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.699 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.371 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.421 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.593 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.565 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.530 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.492 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.591 |
LIG_LIR_Apic_2 | 414 | 420 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 266 | 273 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 59 | 70 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 87 | 97 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.507 |
LIG_MYND_2 | 219 | 223 | PF01753 | 0.532 |
LIG_MYND_3 | 53 | 57 | PF01753 | 0.397 |
LIG_NRP_CendR_1 | 427 | 430 | PF00754 | 0.579 |
LIG_Pex14_1 | 275 | 279 | PF04695 | 0.407 |
LIG_Pex14_1 | 62 | 66 | PF04695 | 0.427 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.430 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.444 |
LIG_SH2_STAT3 | 406 | 409 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.431 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.474 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.539 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.482 |
LIG_SUMO_SIM_anti_2 | 253 | 259 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 219 | 224 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 233 | 240 | PF11976 | 0.484 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.537 |
LIG_TYR_ITIM | 291 | 296 | PF00017 | 0.425 |
LIG_ULM_U2AF65_1 | 85 | 90 | PF00076 | 0.500 |
LIG_WW_2 | 388 | 391 | PF00397 | 0.437 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.753 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.574 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.702 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.443 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.640 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.496 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.452 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.709 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.468 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.616 |
MOD_Cter_Amidation | 410 | 413 | PF01082 | 0.552 |
MOD_Cter_Amidation | 83 | 86 | PF01082 | 0.520 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.474 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.327 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.528 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.379 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.699 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.718 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.588 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.505 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.440 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.615 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.542 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.752 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.465 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.671 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.741 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.808 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.711 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.489 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.570 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.449 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.624 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.666 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.427 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.577 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.537 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.409 |
MOD_PIKK_1 | 419 | 425 | PF00454 | 0.541 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.593 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.656 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.387 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.521 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.538 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.461 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.642 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.413 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.448 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.447 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.391 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.516 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.471 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.433 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.678 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.563 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.673 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.608 |
MOD_SUMO_rev_2 | 189 | 198 | PF00179 | 0.347 |
TRG_DiLeu_BaEn_1 | 212 | 217 | PF01217 | 0.427 |
TRG_DiLeu_LyEn_5 | 212 | 217 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC61 | Leptomonas seymouri | 56% | 67% |
A0A0S4IPB1 | Bodo saltans | 33% | 81% |
A0A3S7XBY9 | Leishmania donovani | 100% | 70% |
A4HQB7 | Leishmania braziliensis | 77% | 100% |
E9AU33 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q0G2 | Leishmania major | 94% | 100% |