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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AXI7
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.678 |
CLV_PCSK_FUR_1 | 153 | 157 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.603 |
DEG_APCC_DBOX_1 | 226 | 234 | PF00400 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 88 | 94 | PF00134 | 0.400 |
DOC_MAPK_gen_1 | 153 | 161 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 6 | 15 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 153 | 161 | PF00069 | 0.481 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.438 |
DOC_PP4_FxxP_1 | 279 | 282 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.633 |
DOC_USP7_UBL2_3 | 45 | 49 | PF12436 | 0.597 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.606 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.725 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 9 | 14 | PF00244 | 0.593 |
LIG_14-3-3_CterR_2 | 439 | 441 | PF00244 | 0.632 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.360 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.481 |
LIG_deltaCOP1_diTrp_1 | 29 | 35 | PF00928 | 0.657 |
LIG_EH_1 | 319 | 323 | PF12763 | 0.664 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.509 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.414 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.426 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.673 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.275 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.579 |
LIG_Integrin_isoDGR_2 | 380 | 382 | PF01839 | 0.751 |
LIG_LIR_Apic_2 | 278 | 282 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 105 | 116 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.503 |
LIG_MYND_1 | 311 | 315 | PF01753 | 0.606 |
LIG_PCNA_yPIPBox_3 | 164 | 178 | PF02747 | 0.548 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.323 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.398 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.572 |
LIG_SH2_NCK_1 | 57 | 61 | PF00017 | 0.572 |
LIG_SH2_PTP2 | 158 | 161 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.504 |
LIG_SH3_1 | 420 | 426 | PF00018 | 0.642 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.658 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.621 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.660 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.581 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.638 |
LIG_SUMO_SIM_par_1 | 141 | 146 | PF11976 | 0.551 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.419 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.596 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.749 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.617 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.573 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.675 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.711 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.635 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.706 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.631 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.593 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.408 |
MOD_Cter_Amidation | 153 | 156 | PF01082 | 0.418 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.439 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.630 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.736 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.787 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.495 |
MOD_GlcNHglycan | 341 | 346 | PF01048 | 0.643 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.749 |
MOD_GlcNHglycan | 412 | 416 | PF01048 | 0.634 |
MOD_GlcNHglycan | 419 | 423 | PF01048 | 0.668 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.551 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.466 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.627 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.663 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.701 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.764 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.616 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.577 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.402 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.814 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.652 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.388 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.699 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.795 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.496 |
MOD_PKA_1 | 300 | 306 | PF00069 | 0.738 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.634 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.720 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.708 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.612 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.392 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.614 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.675 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.600 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.592 |
MOD_Plk_2-3 | 357 | 363 | PF00069 | 0.632 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.552 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.587 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.543 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.621 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.724 |
MOD_SUMO_for_1 | 338 | 341 | PF00179 | 0.657 |
MOD_SUMO_for_1 | 358 | 361 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 351 | 360 | PF00179 | 0.685 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 166 | 171 | PF01217 | 0.558 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.587 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.565 |
TRG_NLS_MonoExtN_4 | 4 | 10 | PF00514 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F7 | Leptomonas seymouri | 65% | 100% |
A0A0S4IKR5 | Bodo saltans | 36% | 100% |
A0A1X0NLV4 | Trypanosomatidae | 44% | 100% |
A0A3R7KUR5 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WZ21 | Leishmania donovani | 95% | 98% |
A4HE44 | Leishmania braziliensis | 83% | 100% |
A4I1F0 | Leishmania infantum | 95% | 98% |
C9ZJX0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
Q4Q9Y5 | Leishmania major | 92% | 100% |
V5BKV0 | Trypanosoma cruzi | 49% | 100% |