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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3Q8ICX1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.414 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.770 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.770 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.439 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.637 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.606 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.798 |
DOC_CYCLIN_RxL_1 | 13 | 21 | PF00134 | 0.643 |
DOC_CYCLIN_yCln2_LP_2 | 158 | 164 | PF00134 | 0.528 |
DOC_MAPK_DCC_7 | 366 | 375 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 366 | 375 | PF00069 | 0.347 |
DOC_PP1_RVXF_1 | 208 | 215 | PF00149 | 0.547 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.688 |
DOC_PP2B_LxvP_1 | 313 | 316 | PF13499 | 0.534 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.706 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.699 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.554 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.763 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 238 | 245 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 298 | 307 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 61 | 71 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 72 | 82 | PF00244 | 0.726 |
LIG_Actin_WH2_2 | 372 | 388 | PF00022 | 0.387 |
LIG_APCC_ABBA_1 | 297 | 302 | PF00400 | 0.427 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_CSL_BTD_1 | 42 | 45 | PF09270 | 0.576 |
LIG_eIF4E_1 | 356 | 362 | PF01652 | 0.473 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.478 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.414 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.530 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.517 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.505 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.490 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.598 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.626 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.464 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.757 |
LIG_FXI_DFP_1 | 300 | 304 | PF00024 | 0.462 |
LIG_GBD_Chelix_1 | 413 | 421 | PF00786 | 0.531 |
LIG_HP1_1 | 371 | 375 | PF01393 | 0.437 |
LIG_LIR_Apic_2 | 199 | 205 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 136 | 147 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 416 | 422 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.606 |
LIG_NRBOX | 14 | 20 | PF00104 | 0.645 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.428 |
LIG_NRBOX | 356 | 362 | PF00104 | 0.510 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.552 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.527 |
LIG_PTAP_UEV_1 | 152 | 157 | PF05743 | 0.504 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.726 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.581 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.613 |
LIG_SH2_GRB2like | 356 | 359 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 118 | 122 | PF00017 | 0.429 |
LIG_SH2_STAT3 | 229 | 232 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.546 |
LIG_SH3_1 | 150 | 156 | PF00018 | 0.519 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.480 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.763 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.788 |
LIG_SH3_CIN85_PxpxPR_1 | 34 | 39 | PF14604 | 0.601 |
LIG_SUMO_SIM_par_1 | 269 | 275 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 370 | 376 | PF11976 | 0.385 |
LIG_UBA3_1 | 287 | 295 | PF00899 | 0.550 |
MOD_CDK_SPK_2 | 290 | 295 | PF00069 | 0.476 |
MOD_CDK_SPK_2 | 361 | 366 | PF00069 | 0.434 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.588 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.559 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.655 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.576 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.587 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.468 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.589 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.664 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.678 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.428 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.665 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.673 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.629 |
MOD_GlcNHglycan | 99 | 104 | PF01048 | 0.800 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.688 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.496 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.709 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.677 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.655 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.581 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.524 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.631 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.505 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.557 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.407 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.578 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.680 |
MOD_NEK2_2 | 333 | 338 | PF00069 | 0.467 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.610 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.579 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.682 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.452 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.573 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.653 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.617 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.572 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.513 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.348 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.461 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.459 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.657 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.596 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.616 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.513 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.602 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.469 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.508 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.762 |
MOD_SUMO_rev_2 | 219 | 228 | PF00179 | 0.540 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.614 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.734 |
TRG_Pf-PMV_PEXEL_1 | 16 | 20 | PF00026 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7E4 | Leptomonas seymouri | 41% | 91% |
A0A1X0NTZ3 | Trypanosomatidae | 32% | 100% |
A0A3R7L6E6 | Trypanosoma rangeli | 29% | 100% |
A4HEW5 | Leishmania braziliensis | 76% | 100% |
A4I238 | Leishmania infantum | 99% | 100% |
C9ZRW6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AY88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q985 | Leishmania major | 91% | 100% |