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: Q4QAG5
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 | 212 | 216 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 250 | 254 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.655 |
CLV_PCSK_FUR_1 | 28 | 32 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.764 |
CLV_PCSK_PC7_1 | 10 | 16 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.344 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.676 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.734 |
DEG_SCF_FBW7_2 | 121 | 126 | PF00400 | 0.630 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.762 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.561 |
DOC_CKS1_1 | 494 | 499 | PF01111 | 0.600 |
DOC_CYCLIN_RxL_1 | 203 | 212 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 106 | 112 | PF00134 | 0.570 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.674 |
DOC_MAPK_RevD_3 | 193 | 206 | PF00069 | 0.516 |
DOC_PP2B_LxvP_1 | 234 | 237 | PF13499 | 0.607 |
DOC_PP2B_LxvP_1 | 291 | 294 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 367 | 370 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 448 | 451 | PF13499 | 0.518 |
DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.392 |
DOC_SPAK_OSR1_1 | 383 | 387 | PF12202 | 0.580 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.799 |
DOC_USP7_UBL2_3 | 143 | 147 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.796 |
LIG_14-3-3_CanoR_1 | 102 | 107 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 327 | 334 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 90 | 99 | PF00244 | 0.719 |
LIG_Actin_WH2_2 | 286 | 304 | PF00022 | 0.562 |
LIG_AP2alpha_2 | 275 | 277 | PF02296 | 0.620 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.651 |
LIG_EH1_1 | 279 | 287 | PF00400 | 0.517 |
LIG_eIF4E_1 | 309 | 315 | PF01652 | 0.562 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.518 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.329 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.395 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.442 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.397 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.551 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.506 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.521 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.575 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.791 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.574 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.654 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.704 |
LIG_Integrin_isoDGR_2 | 436 | 438 | PF01839 | 0.321 |
LIG_LIR_Apic_2 | 220 | 224 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 477 | 485 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.431 |
LIG_LRP6_Inhibitor_1 | 223 | 229 | PF00058 | 0.358 |
LIG_MYND_1 | 84 | 88 | PF01753 | 0.726 |
LIG_PDZ_Class_1 | 513 | 518 | PF00595 | 0.786 |
LIG_Pex14_1 | 439 | 443 | PF04695 | 0.517 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.395 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.743 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.701 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.382 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.648 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.487 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 421 | 428 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 480 | 486 | PF11976 | 0.564 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.641 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.562 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.562 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.537 |
LIG_WRC_WIRS_1 | 455 | 460 | PF05994 | 0.536 |
LIG_WW_3 | 414 | 418 | PF00397 | 0.418 |
MOD_CDK_SPxxK_3 | 332 | 339 | PF00069 | 0.500 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.703 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.522 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.537 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.558 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.714 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.760 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.753 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.425 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.477 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.419 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.741 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.525 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.455 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.459 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.538 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.785 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.627 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.537 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.527 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.806 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.500 |
MOD_LATS_1 | 100 | 106 | PF00433 | 0.446 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.300 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.441 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.684 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.529 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.504 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.594 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.562 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.500 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.560 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.730 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.419 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.765 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.476 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.559 |
MOD_PKB_1 | 102 | 110 | PF00069 | 0.559 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.538 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.565 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.517 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.557 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.446 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.537 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.562 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.487 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.482 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.388 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.500 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.579 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.796 |
MOD_SUMO_rev_2 | 60 | 70 | PF00179 | 0.668 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.765 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1U8 | Leptomonas seymouri | 61% | 100% |
A0A0S4JI78 | Bodo saltans | 41% | 100% |
A0A1X0NVU0 | Trypanosomatidae | 45% | 100% |
A0A3Q8IBF1 | Leishmania donovani | 91% | 100% |
A0A3R7R8W6 | Trypanosoma rangeli | 45% | 100% |
A4HDM6 | Leishmania braziliensis | 81% | 100% |
C9ZWD9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AH73 | Leishmania infantum | 91% | 100% |
E9AX11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BFK4 | Trypanosoma cruzi | 45% | 100% |