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:0016604 | nuclear body | 2 | 12 |
GO:0016605 | PML body | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005634 | nucleus | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4H5J1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0016567 | protein ubiquitination | 7 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0032446 | protein modification by small protein conjugation | 6 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.484 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.169 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 518 | 520 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.410 |
DEG_APCC_DBOX_1 | 419 | 427 | PF00400 | 0.169 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.394 |
DOC_CYCLIN_RxL_1 | 417 | 425 | PF00134 | 0.169 |
DOC_CYCLIN_RxL_1 | 464 | 471 | PF00134 | 0.255 |
DOC_CYCLIN_yCln2_LP_2 | 38 | 44 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 116 | 126 | PF00069 | 0.255 |
DOC_MAPK_RevD_3 | 101 | 117 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 465 | 471 | PF00149 | 0.169 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.581 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.345 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.311 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.232 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.345 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 250 | 259 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 459 | 465 | PF00244 | 0.460 |
LIG_APCC_ABBA_1 | 385 | 390 | PF00400 | 0.332 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.623 |
LIG_EVH1_2 | 398 | 402 | PF00568 | 0.345 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.343 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.280 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.397 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.398 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.209 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.443 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.315 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.169 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.376 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.169 |
LIG_Integrin_isoDGR_2 | 114 | 116 | PF01839 | 0.307 |
LIG_LIR_Apic_2 | 187 | 192 | PF02991 | 0.397 |
LIG_LIR_Apic_2 | 329 | 334 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 463 | 472 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.314 |
LIG_PCNA_PIPBox_1 | 409 | 418 | PF02747 | 0.251 |
LIG_PCNA_yPIPBox_3 | 409 | 420 | PF02747 | 0.183 |
LIG_PCNA_yPIPBox_3 | 451 | 465 | PF02747 | 0.365 |
LIG_PTB_Apo_2 | 362 | 369 | PF02174 | 0.218 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.251 |
LIG_SH3_2 | 384 | 389 | PF14604 | 0.281 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.375 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.443 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.484 |
LIG_UBA3_1 | 163 | 168 | PF00899 | 0.466 |
MOD_CDK_SPxxK_3 | 11 | 18 | PF00069 | 0.607 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.483 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.606 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.271 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.386 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.295 |
MOD_Cter_Amidation | 114 | 117 | PF01082 | 0.348 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.635 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.590 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.499 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.332 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.375 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.480 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.293 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.287 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.550 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.419 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.514 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.373 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.233 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.313 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.551 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.451 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.251 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.280 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.300 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.354 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.448 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.345 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.449 |
MOD_PK_1 | 191 | 197 | PF00069 | 0.345 |
MOD_PK_1 | 392 | 398 | PF00069 | 0.169 |
MOD_PKA_1 | 250 | 256 | PF00069 | 0.307 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.464 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.321 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.332 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.425 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.251 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.268 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.258 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.239 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.307 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.636 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.682 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.394 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.345 |
MOD_SUMO_for_1 | 119 | 122 | PF00179 | 0.386 |
MOD_SUMO_for_1 | 167 | 170 | PF00179 | 0.484 |
TRG_DiLeu_BaEn_4 | 254 | 260 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.169 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.304 |
TRG_NES_CRM1_1 | 91 | 105 | PF08389 | 0.281 |
TRG_NLS_MonoExtC_3 | 273 | 279 | PF00514 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 420 | 424 | PF00026 | 0.169 |
TRG_Pf-PMV_PEXEL_1 | 467 | 471 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P377 | Leptomonas seymouri | 63% | 97% |
A0A0S4JT63 | Bodo saltans | 40% | 100% |
A0A1X0NPC5 | Trypanosomatidae | 43% | 98% |
A0A3R7MDE3 | Trypanosoma rangeli | 42% | 95% |
A0A3S5H6B1 | Leishmania donovani | 75% | 99% |
A4HTT2 | Leishmania infantum | 75% | 99% |
A5WW08 | Danio rerio | 31% | 82% |
D0A993 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 94% |
E9AML5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |
Q4QI21 | Leishmania major | 75% | 100% |
Q5FWP4 | Xenopus laevis | 29% | 83% |
Q5RF77 | Pongo abelii | 26% | 91% |
Q6P256 | Xenopus tropicalis | 29% | 83% |
Q810L3 | Mus musculus | 28% | 78% |
Q96EP1 | Homo sapiens | 27% | 78% |
V5DJC2 | Trypanosoma cruzi | 42% | 83% |