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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0016020 | membrane | 2 | 4 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: Q4QJA9
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016874 | ligase activity | 2 | 4 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0061631 | ubiquitin conjugating enzyme activity | 5 | 2 |
GO:0061650 | ubiquitin-like protein conjugating enzyme activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.457 |
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.304 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.660 |
DEG_APCC_DBOX_1 | 454 | 462 | PF00400 | 0.440 |
DEG_SCF_FBW7_1 | 193 | 200 | PF00400 | 0.451 |
DEG_SCF_FBW7_1 | 225 | 232 | PF00400 | 0.475 |
DEG_SCF_FBW7_2 | 360 | 367 | PF00400 | 0.466 |
DOC_CKS1_1 | 194 | 199 | PF01111 | 0.452 |
DOC_CKS1_1 | 289 | 294 | PF01111 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 233 | 236 | PF00134 | 0.453 |
DOC_MAPK_RevD_3 | 42 | 58 | PF00069 | 0.222 |
DOC_MAPK_RevD_3 | 442 | 456 | PF00069 | 0.366 |
DOC_PP1_RVXF_1 | 419 | 425 | PF00149 | 0.430 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.269 |
DOC_SPAK_OSR1_1 | 86 | 90 | PF12202 | 0.316 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.464 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 456 | 462 | PF00244 | 0.237 |
LIG_Actin_WH2_2 | 442 | 457 | PF00022 | 0.396 |
LIG_APCC_ABBA_1 | 170 | 175 | PF00400 | 0.376 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.372 |
LIG_BIR_III_2 | 380 | 384 | PF00653 | 0.460 |
LIG_BRCT_BRCA1_1 | 444 | 448 | PF00533 | 0.279 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.316 |
LIG_CtBP_PxDLS_1 | 356 | 360 | PF00389 | 0.418 |
LIG_deltaCOP1_diTrp_1 | 144 | 153 | PF00928 | 0.349 |
LIG_deltaCOP1_diTrp_1 | 39 | 42 | PF00928 | 0.269 |
LIG_EH1_1 | 447 | 455 | PF00400 | 0.272 |
LIG_EVH1_1 | 187 | 191 | PF00568 | 0.492 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.269 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.377 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.546 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.494 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.451 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.554 |
LIG_GBD_Chelix_1 | 443 | 451 | PF00786 | 0.323 |
LIG_LIR_Apic_2 | 27 | 32 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 445 | 454 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.305 |
LIG_MYND_1 | 185 | 189 | PF01753 | 0.441 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.351 |
LIG_Pex14_1 | 105 | 109 | PF04695 | 0.269 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.269 |
LIG_PROFILIN_1 | 188 | 194 | PF00235 | 0.455 |
LIG_REV1ctd_RIR_1 | 78 | 87 | PF16727 | 0.269 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.268 |
LIG_SH2_PTP2 | 29 | 32 | PF00017 | 0.284 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.284 |
LIG_SH3_1 | 186 | 192 | PF00018 | 0.461 |
LIG_SH3_1 | 260 | 266 | PF00018 | 0.493 |
LIG_SH3_1 | 69 | 75 | PF00018 | 0.294 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.480 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.469 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.504 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.481 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.465 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.481 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.471 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.476 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.426 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.460 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.433 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.294 |
LIG_TRFH_1 | 71 | 75 | PF08558 | 0.304 |
LIG_WRC_WIRS_1 | 443 | 448 | PF05994 | 0.325 |
MOD_CDC14_SPxK_1 | 177 | 180 | PF00782 | 0.553 |
MOD_CDC14_SPxK_1 | 327 | 330 | PF00782 | 0.638 |
MOD_CDK_SPxK_1 | 174 | 180 | PF00069 | 0.539 |
MOD_CDK_SPxK_1 | 324 | 330 | PF00069 | 0.636 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.397 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.546 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.304 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.451 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.644 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.624 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.693 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.610 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.447 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.339 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.496 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.393 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.609 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.670 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.560 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.237 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.324 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.304 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.553 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.608 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.551 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.330 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.307 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.329 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.418 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.579 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.304 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.341 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.304 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.545 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.316 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.617 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.554 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.620 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.571 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.369 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.210 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.543 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.516 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.822 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.614 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.658 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.668 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.619 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.674 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.578 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.555 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.528 |
MOD_SUMO_for_1 | 203 | 206 | PF00179 | 0.630 |
TRG_DiLeu_BaLyEn_6 | 433 | 438 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1C5 | Leptomonas seymouri | 43% | 95% |
A0A3S5H5K9 | Leishmania donovani | 81% | 100% |
A4H4D6 | Leishmania braziliensis | 60% | 100% |
A4HSL5 | Leishmania infantum | 81% | 100% |
E9AKJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |