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 |
Related structures:
AlphaFold database: E9AH73
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 211 | 215 | PF00656 | 0.369 |
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.730 |
CLV_PCSK_FUR_1 | 28 | 32 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.250 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.303 |
CLV_PCSK_PC7_1 | 10 | 16 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.389 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.588 |
DEG_SCF_FBW7_2 | 120 | 125 | PF00400 | 0.506 |
DEG_SCF_TRCP1_1 | 179 | 184 | PF00400 | 0.334 |
DEG_SPOP_SBC_1 | 59 | 63 | PF00917 | 0.602 |
DOC_CYCLIN_RxL_1 | 202 | 211 | PF00134 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 272 | 278 | PF00134 | 0.623 |
DOC_CYCLIN_yCln2_LP_2 | 491 | 494 | PF00134 | 0.432 |
DOC_MAPK_DCC_7 | 94 | 102 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 94 | 102 | PF00069 | 0.434 |
DOC_MAPK_RevD_3 | 192 | 205 | PF00069 | 0.489 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.486 |
DOC_PP2B_LxvP_1 | 290 | 293 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 366 | 369 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 491 | 494 | PF13499 | 0.455 |
DOC_PP4_FxxP_1 | 220 | 223 | PF00568 | 0.342 |
DOC_SPAK_OSR1_1 | 382 | 386 | PF12202 | 0.488 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.736 |
DOC_USP7_UBL2_3 | 142 | 146 | PF12436 | 0.446 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.753 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 326 | 333 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.624 |
LIG_Actin_WH2_2 | 16 | 32 | PF00022 | 0.495 |
LIG_Actin_WH2_2 | 285 | 303 | PF00022 | 0.538 |
LIG_AP2alpha_2 | 274 | 276 | PF02296 | 0.522 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.538 |
LIG_EH1_1 | 278 | 286 | PF00400 | 0.489 |
LIG_eIF4E_1 | 308 | 314 | PF01652 | 0.538 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.487 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.291 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.408 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.442 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.432 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.372 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.534 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.467 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.452 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.345 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.560 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.443 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.499 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.657 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.542 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.481 |
LIG_Integrin_isoDGR_2 | 435 | 437 | PF01839 | 0.252 |
LIG_LIR_Apic_2 | 219 | 223 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 476 | 484 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.389 |
LIG_MYND_1 | 83 | 87 | PF01753 | 0.604 |
LIG_PDZ_Class_1 | 513 | 518 | PF00595 | 0.647 |
LIG_Pex14_1 | 438 | 442 | PF04695 | 0.478 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.503 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.655 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.363 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.601 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.669 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.330 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.619 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.535 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.490 |
LIG_SUMO_SIM_par_1 | 106 | 113 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 420 | 427 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 479 | 485 | PF11976 | 0.536 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.612 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.538 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.538 |
LIG_TYR_ITIM | 440 | 445 | PF00017 | 0.503 |
MOD_CDK_SPxxK_3 | 331 | 338 | PF00069 | 0.460 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.598 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.503 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.526 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.461 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.543 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.486 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.720 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.710 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.365 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.400 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.359 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.586 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.613 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.737 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.240 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.347 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.505 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.426 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.402 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.333 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.501 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.787 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.546 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.503 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.491 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.543 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.480 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.472 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.417 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.272 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.505 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.403 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.601 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.717 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.523 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.501 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.574 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.538 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.460 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.539 |
MOD_PKA_1 | 30 | 36 | PF00069 | 0.522 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.386 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.730 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.436 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.417 |
MOD_PKB_1 | 101 | 109 | PF00069 | 0.446 |
MOD_PKB_1 | 28 | 36 | PF00069 | 0.519 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.503 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.563 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.488 |
MOD_Plk_2-3 | 47 | 53 | PF00069 | 0.501 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.420 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.503 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.538 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.462 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.430 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.334 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.460 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.755 |
MOD_SUMO_rev_2 | 62 | 70 | PF00179 | 0.545 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.663 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.717 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.627 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1U8 | Leptomonas seymouri | 63% | 100% |
A0A0S4JI78 | Bodo saltans | 42% | 100% |
A0A1X0NVU0 | Trypanosomatidae | 44% | 100% |
A0A3Q8IBF1 | Leishmania donovani | 99% | 100% |
A0A3R7R8W6 | Trypanosoma rangeli | 45% | 100% |
A4HDM6 | Leishmania braziliensis | 79% | 100% |
C9ZWD9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AX11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QAG5 | Leishmania major | 91% | 100% |
V5BFK4 | Trypanosoma cruzi | 46% | 100% |