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:0005739 | mitochondrion | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9AWA4
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0010257 | NADH dehydrogenase complex assembly | 6 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0032981 | mitochondrial respiratory chain complex I assembly | 7 | 1 |
GO:0033108 | mitochondrial respiratory chain complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0008170 | N-methyltransferase activity | 5 | 10 |
GO:0008276 | protein methyltransferase activity | 3 | 10 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 10 |
GO:0016273 | arginine N-methyltransferase activity | 6 | 10 |
GO:0016274 | protein-arginine N-methyltransferase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
GO:0035243 | protein-arginine omega-N symmetric methyltransferase activity | 5 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 434 | 438 | PF00656 | 0.204 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.409 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.272 |
CLV_PCSK_PC7_1 | 201 | 207 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.341 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.238 |
DEG_APCC_DBOX_1 | 372 | 380 | PF00400 | 0.252 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.431 |
DOC_CKS1_1 | 152 | 157 | PF01111 | 0.230 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.445 |
DOC_CKS1_1 | 62 | 67 | PF01111 | 0.463 |
DOC_CYCLIN_RxL_1 | 151 | 162 | PF00134 | 0.252 |
DOC_MAPK_gen_1 | 217 | 224 | PF00069 | 0.230 |
DOC_MAPK_gen_1 | 296 | 305 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 47 | 55 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 215 | 221 | PF00149 | 0.230 |
DOC_PP1_RVXF_1 | 368 | 375 | PF00149 | 0.230 |
DOC_PP1_RVXF_1 | 382 | 389 | PF00149 | 0.267 |
DOC_PP4_FxxP_1 | 351 | 354 | PF00568 | 0.230 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.240 |
DOC_USP7_UBL2_3 | 417 | 421 | PF12436 | 0.358 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.480 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 251 | 258 | PF00244 | 0.230 |
LIG_14-3-3_CanoR_1 | 67 | 71 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 7 | 12 | PF00244 | 0.444 |
LIG_Actin_WH2_2 | 360 | 375 | PF00022 | 0.230 |
LIG_BIR_III_2 | 243 | 247 | PF00653 | 0.230 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.252 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.290 |
LIG_eIF4E_1 | 180 | 186 | PF01652 | 0.230 |
LIG_EVH1_1 | 461 | 465 | PF00568 | 0.452 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.274 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.206 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.307 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.230 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.291 |
LIG_LIR_Apic_2 | 285 | 290 | PF02991 | 0.230 |
LIG_LIR_Gen_1 | 147 | 157 | PF02991 | 0.230 |
LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.230 |
LIG_LIR_Gen_1 | 364 | 372 | PF02991 | 0.230 |
LIG_LIR_Gen_1 | 453 | 464 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.337 |
LIG_MLH1_MIPbox_1 | 452 | 456 | PF16413 | 0.290 |
LIG_MYND_1 | 354 | 358 | PF01753 | 0.230 |
LIG_NRP_CendR_1 | 467 | 470 | PF00754 | 0.643 |
LIG_PTB_Apo_2 | 236 | 243 | PF02174 | 0.230 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.230 |
LIG_SH2_CRK | 426 | 430 | PF00017 | 0.301 |
LIG_SH2_GRB2like | 180 | 183 | PF00017 | 0.230 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.230 |
LIG_SH3_2 | 462 | 467 | PF14604 | 0.426 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.606 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.288 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.633 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.437 |
LIG_TRFH_1 | 229 | 233 | PF08558 | 0.252 |
LIG_UBA3_1 | 170 | 176 | PF00899 | 0.230 |
LIG_UBA3_1 | 316 | 325 | PF00899 | 0.230 |
LIG_WW_2 | 462 | 465 | PF00397 | 0.485 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.230 |
MOD_CDK_SPxK_1 | 46 | 52 | PF00069 | 0.602 |
MOD_CDK_SPxK_1 | 61 | 67 | PF00069 | 0.412 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.511 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.459 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.322 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.234 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.230 |
MOD_Cter_Amidation | 296 | 299 | PF01082 | 0.144 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.734 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.230 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.230 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.568 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.345 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.291 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.736 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.297 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.167 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.230 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.456 |
MOD_N-GLC_1 | 450 | 455 | PF02516 | 0.283 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.297 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.422 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.230 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.282 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.505 |
MOD_NEK2_2 | 365 | 370 | PF00069 | 0.345 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.279 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.273 |
MOD_PK_1 | 7 | 13 | PF00069 | 0.427 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.401 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.230 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.261 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.561 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.446 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.230 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.627 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.230 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.285 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.371 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.230 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.632 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.230 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.347 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.602 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.412 |
MOD_SUMO_for_1 | 411 | 414 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 202 | 207 | PF00179 | 0.252 |
MOD_SUMO_rev_2 | 413 | 419 | PF00179 | 0.372 |
MOD_SUMO_rev_2 | 72 | 81 | PF00179 | 0.377 |
TRG_DiLeu_BaEn_2 | 123 | 129 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_2 | 231 | 237 | PF01217 | 0.252 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.230 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.290 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.345 |
TRG_ER_FFAT_2 | 123 | 133 | PF00635 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.238 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT9 | Leptomonas seymouri | 88% | 95% |
A0A1X0NXJ4 | Trypanosomatidae | 81% | 100% |
A0A3S7WXU3 | Leishmania donovani | 97% | 100% |
A4HCW1 | Leishmania braziliensis | 96% | 100% |
A4I0E1 | Leishmania infantum | 97% | 100% |
C9ZV33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 77% | 100% |
Q08BY0 | Danio rerio | 30% | 100% |
Q09644 | Caenorhabditis elegans | 28% | 100% |
Q2KHV5 | Bos taurus | 30% | 100% |
Q4QB74 | Leishmania major | 97% | 100% |
Q54S83 | Dictyostelium discoideum | 35% | 97% |
Q5BKM6 | Xenopus tropicalis | 32% | 100% |
Q5XI79 | Rattus norvegicus | 32% | 100% |
Q6GQ37 | Xenopus laevis | 31% | 100% |
Q7L592 | Homo sapiens | 33% | 100% |
Q9CWG8 | Mus musculus | 33% | 100% |
Q9VGR2 | Drosophila melanogaster | 29% | 100% |
V5D7M8 | Trypanosoma cruzi | 81% | 100% |