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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 9 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0008173 | RNA methyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.326 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.432 |
CLV_PCSK_FUR_1 | 381 | 385 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.418 |
CLV_PCSK_PC7_1 | 276 | 282 | PF00082 | 0.422 |
CLV_PCSK_PC7_1 | 410 | 416 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.493 |
CLV_Separin_Metazoa | 378 | 382 | PF03568 | 0.497 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.365 |
DEG_APCC_DBOX_1 | 275 | 283 | PF00400 | 0.598 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.411 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.273 |
DEG_SPOP_SBC_1 | 226 | 230 | PF00917 | 0.511 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.515 |
DOC_CYCLIN_RxL_1 | 80 | 93 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 285 | 295 | PF00069 | 0.462 |
DOC_MAPK_JIP1_4 | 19 | 25 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 344 | 352 | PF00069 | 0.533 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.472 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.374 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.412 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 354 | 364 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.626 |
LIG_eIF4E_1 | 18 | 24 | PF01652 | 0.292 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.506 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.395 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.452 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.527 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.436 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.435 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.529 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.571 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.516 |
LIG_IRF3_LxIS_1 | 305 | 311 | PF10401 | 0.449 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.426 |
LIG_LIR_Apic_2 | 457 | 463 | PF02991 | 0.575 |
LIG_LIR_Apic_2 | 64 | 68 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 264 | 272 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.483 |
LIG_NRP_CendR_1 | 462 | 465 | PF00754 | 0.591 |
LIG_PCNA_yPIPBox_3 | 401 | 415 | PF02747 | 0.563 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.446 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.353 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.692 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.435 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.405 |
LIG_SH3_2 | 68 | 73 | PF14604 | 0.401 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.669 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.694 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.474 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.426 |
LIG_SH3_CIN85_PxpxPR_1 | 214 | 219 | PF14604 | 0.641 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.320 |
LIG_TRFH_1 | 317 | 321 | PF08558 | 0.420 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.460 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.497 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.577 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.394 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.540 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.342 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.566 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.674 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.489 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.425 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.407 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.415 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.626 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.520 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.555 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.494 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.282 |
MOD_LATS_1 | 452 | 458 | PF00433 | 0.568 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.230 |
MOD_N-GLC_2 | 117 | 119 | PF02516 | 0.282 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.315 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.670 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.559 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.541 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.423 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.385 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.546 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.666 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.474 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.610 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.610 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.545 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.438 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.555 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.582 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.629 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.475 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.604 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.413 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.643 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.447 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.282 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.551 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.431 |
MOD_SUMO_for_1 | 145 | 148 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 256 | 264 | PF00179 | 0.394 |
TRG_DiLeu_BaEn_1 | 162 | 167 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_4 | 334 | 340 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 319 | 322 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 85 | 90 | PF00026 | 0.282 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEE8 | Leptomonas seymouri | 70% | 76% |
A0A1X0P5S3 | Trypanosomatidae | 50% | 80% |
A0A3S7X9F7 | Leishmania donovani | 82% | 77% |
A0A422P2S4 | Trypanosoma rangeli | 48% | 82% |
A4IBH7 | Leishmania infantum | 82% | 77% |
C9ZZ65 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 79% |
E9AFB3 | Leishmania major | 80% | 100% |
E9B6G8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 77% |