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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HB46
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007264 | small GTPase mediated signal transduction | 4 | 1 |
GO:0007265 | Ras protein signal transduction | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular 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:0035556 | intracellular signal transduction | 3 | 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:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 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 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 2 |
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 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.562 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.707 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.519 |
DEG_SPOP_SBC_1 | 107 | 111 | PF00917 | 0.396 |
DOC_MAPK_MEF2A_6 | 158 | 166 | PF00069 | 0.513 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.560 |
DOC_USP7_UBL2_3 | 269 | 273 | PF12436 | 0.480 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 408 | 416 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.568 |
LIG_Actin_WH2_2 | 35 | 52 | PF00022 | 0.341 |
LIG_Actin_WH2_2 | 381 | 398 | PF00022 | 0.498 |
LIG_Actin_WH2_2 | 402 | 419 | PF00022 | 0.510 |
LIG_AP2alpha_2 | 161 | 163 | PF02296 | 0.463 |
LIG_EH1_1 | 210 | 218 | PF00400 | 0.631 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.559 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.450 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.613 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.545 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.329 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.590 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.446 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.635 |
LIG_LIR_Apic_2 | 75 | 81 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 223 | 230 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 335 | 343 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 335 | 339 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.504 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.595 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.590 |
LIG_SH2_STAT3 | 97 | 100 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.488 |
LIG_SH3_1 | 78 | 84 | PF00018 | 0.577 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 31 | 37 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 212 | 221 | PF11976 | 0.532 |
LIG_TYR_ITSM | 73 | 80 | PF00017 | 0.531 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.631 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.671 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.578 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.563 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.491 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.560 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.626 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.491 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.686 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.660 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.618 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.651 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.665 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.564 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.476 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.612 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.690 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.564 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.623 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.523 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.397 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.483 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.595 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.560 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.627 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.471 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.396 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.379 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.574 |
MOD_OFUCOSY | 117 | 123 | PF10250 | 0.447 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.407 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.454 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.596 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.576 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.663 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.641 |
MOD_PKA_1 | 358 | 364 | PF00069 | 0.576 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.398 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.490 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.600 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.588 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.510 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.675 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.475 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.560 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.597 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.634 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.716 |
MOD_SUMO_for_1 | 151 | 154 | PF00179 | 0.512 |
MOD_SUMO_for_1 | 285 | 288 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 257 | 266 | PF00179 | 0.646 |
MOD_SUMO_rev_2 | 267 | 275 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 287 | 294 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 410 | 419 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_4 | 379 | 385 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 431 | 436 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAV0 | Leptomonas seymouri | 65% | 80% |
A0A0S4ILW6 | Bodo saltans | 31% | 84% |
A0A1X0PAX0 | Trypanosomatidae | 33% | 94% |
A0A3Q8IEL0 | Leishmania donovani | 83% | 100% |
A0A422NNH1 | Trypanosoma rangeli | 37% | 97% |
A4IA95 | Leishmania infantum | 83% | 82% |
C9ZLZ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 97% |
E9B5B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
O13747 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 88% |
Q4Q2L6 | Leishmania major | 79% | 100% |
Q7Z569 | Homo sapiens | 24% | 81% |
Q95QN6 | Caenorhabditis elegans | 25% | 81% |
Q99MP8 | Mus musculus | 24% | 81% |
V5DLZ1 | Trypanosoma cruzi | 33% | 95% |