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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AK36
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 13 |
GO:0005509 | calcium ion binding | 5 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
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:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 193 | 197 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.424 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.532 |
CLV_PCSK_FUR_1 | 570 | 574 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 571 | 573 | PF00082 | 0.522 |
CLV_PCSK_PC7_1 | 157 | 163 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.433 |
DEG_APCC_DBOX_1 | 277 | 285 | PF00400 | 0.348 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.404 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.416 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.508 |
DOC_CYCLIN_RxL_1 | 68 | 77 | PF00134 | 0.427 |
DOC_MAPK_gen_1 | 68 | 75 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 293 | 301 | PF00069 | 0.388 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.441 |
DOC_PP2B_LxvP_1 | 446 | 449 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 515 | 518 | PF13499 | 0.613 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.359 |
DOC_PP4_FxxP_1 | 55 | 58 | PF00568 | 0.320 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.530 |
DOC_USP7_MATH_2 | 203 | 209 | PF00917 | 0.601 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 347 | 351 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 451 | 457 | PF00244 | 0.507 |
LIG_APCC_ABBA_1 | 188 | 193 | PF00400 | 0.502 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 475 | 479 | PF00533 | 0.584 |
LIG_CtBP_PxDLS_1 | 23 | 27 | PF00389 | 0.296 |
LIG_EVH1_2 | 417 | 421 | PF00568 | 0.432 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.672 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.373 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.396 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.407 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.556 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.536 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.306 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.439 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.570 |
LIG_Integrin_RGD_1 | 576 | 578 | PF01839 | 0.565 |
LIG_LIR_Apic_2 | 18 | 23 | PF02991 | 0.340 |
LIG_LIR_Apic_2 | 502 | 507 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 54 | 58 | PF02991 | 0.216 |
LIG_LIR_Apic_2 | 8 | 14 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 298 | 307 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 390 | 399 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.447 |
LIG_Pex14_2 | 286 | 290 | PF04695 | 0.408 |
LIG_PROFILIN_1 | 148 | 154 | PF00235 | 0.494 |
LIG_Rb_pABgroove_1 | 263 | 271 | PF01858 | 0.418 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.553 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.704 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.554 |
LIG_SH2_NCK_1 | 504 | 508 | PF00017 | 0.517 |
LIG_SH2_PTP2 | 171 | 174 | PF00017 | 0.610 |
LIG_SH2_PTP2 | 392 | 395 | PF00017 | 0.383 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.610 |
LIG_SH2_SRC | 504 | 507 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.387 |
LIG_SH2_STAT3 | 311 | 314 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.430 |
LIG_SH3_1 | 504 | 510 | PF00018 | 0.511 |
LIG_SH3_2 | 511 | 516 | PF14604 | 0.609 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.810 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.620 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.679 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.658 |
LIG_SUMO_SIM_anti_2 | 123 | 129 | PF11976 | 0.485 |
LIG_SUMO_SIM_anti_2 | 22 | 28 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 294 | 303 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 77 | 82 | PF11976 | 0.361 |
LIG_TRAF2_2 | 3 | 8 | PF00917 | 0.414 |
LIG_UBA3_1 | 300 | 309 | PF00899 | 0.414 |
LIG_WRC_WIRS_1 | 52 | 57 | PF05994 | 0.200 |
MOD_CAAXbox | 581 | 584 | PF01239 | 0.637 |
MOD_CDC14_SPxK_1 | 189 | 192 | PF00782 | 0.588 |
MOD_CDK_SPxK_1 | 186 | 192 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 553 | 560 | PF00069 | 0.610 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.643 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.644 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.560 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.583 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.798 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.243 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.757 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.566 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.503 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.517 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.383 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.410 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.380 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.588 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.656 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.708 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.658 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.655 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.533 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.433 |
MOD_GlcNHglycan | 327 | 331 | PF01048 | 0.432 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.668 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.613 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.600 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.553 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.570 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.686 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.707 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.575 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.779 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.688 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.521 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.338 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.412 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.559 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.593 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.529 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.464 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.560 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.448 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.434 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.668 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.642 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.490 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.524 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.599 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.545 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.486 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.348 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.458 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.578 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.410 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.462 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.530 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.434 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.355 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.605 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.612 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.506 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.371 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.297 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.588 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.450 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.727 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.646 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.500 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.511 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.415 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.447 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.779 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.602 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.638 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.751 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.623 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.377 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.615 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.487 |
MOD_ProDKin_1 | 553 | 559 | PF00069 | 0.578 |
MOD_SUMO_rev_2 | 66 | 70 | PF00179 | 0.413 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.631 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.588 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 165 | 169 | PF00026 | 0.600 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HV78 | Leptomonas seymouri | 48% | 93% |
A0A3Q8IMS6 | Leishmania donovani | 30% | 100% |
A0A3R7KFH5 | Trypanosoma rangeli | 28% | 100% |
A0A3S5H5B1 | Leishmania donovani | 80% | 99% |
A4HDK3 | Leishmania braziliensis | 28% | 97% |
A4HDK4 | Leishmania braziliensis | 28% | 95% |
A4HS49 | Leishmania infantum | 79% | 99% |
A4I0X7 | Leishmania infantum | 27% | 100% |
E9AWY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O97201 | Leishmania major | 77% | 100% |
Q4QAJ3 | Leishmania major | 29% | 91% |