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 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HIJ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009056 | catabolic process | 2 | 13 |
GO:0009057 | macromolecule catabolic process | 4 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0030163 | protein catabolic process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 13 |
GO:1901575 | organic substance catabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0008914 | leucyltransferase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016746 | acyltransferase activity | 3 | 13 |
GO:0016755 | aminoacyltransferase activity | 3 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.610 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.679 |
CLV_Separin_Metazoa | 443 | 447 | PF03568 | 0.261 |
DEG_ODPH_VHL_1 | 14 | 26 | PF01847 | 0.442 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.624 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.556 |
DOC_MAPK_DCC_7 | 457 | 465 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 457 | 465 | PF00069 | 0.255 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.542 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.315 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 237 | 241 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 320 | 324 | PF00244 | 0.502 |
LIG_APCC_ABBA_1 | 475 | 480 | PF00400 | 0.397 |
LIG_BIR_III_2 | 458 | 462 | PF00653 | 0.417 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 37 | 41 | PF00533 | 0.622 |
LIG_Clathr_ClatBox_1 | 362 | 366 | PF01394 | 0.451 |
LIG_CtBP_PxDLS_1 | 151 | 155 | PF00389 | 0.658 |
LIG_CtBP_PxDLS_1 | 215 | 219 | PF00389 | 0.426 |
LIG_deltaCOP1_diTrp_1 | 205 | 212 | PF00928 | 0.364 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.602 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.635 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.440 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.573 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.422 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.402 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.457 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.545 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.434 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.302 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.668 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.630 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.527 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.590 |
LIG_LIR_Apic_2 | 145 | 151 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 290 | 301 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 326 | 332 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.376 |
LIG_PCNA_TLS_4 | 400 | 409 | PF02747 | 0.477 |
LIG_PCNA_yPIPBox_3 | 279 | 288 | PF02747 | 0.419 |
LIG_PCNA_yPIPBox_3 | 71 | 81 | PF02747 | 0.517 |
LIG_Pex14_1 | 423 | 427 | PF04695 | 0.326 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.472 |
LIG_Pex14_2 | 449 | 453 | PF04695 | 0.256 |
LIG_PTAP_UEV_1 | 246 | 251 | PF05743 | 0.451 |
LIG_Rb_LxCxE_1 | 359 | 374 | PF01857 | 0.439 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.304 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.348 |
LIG_SH2_SRC | 188 | 191 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.291 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 435 | 439 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 431 | 434 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.333 |
LIG_SH3_2 | 274 | 279 | PF14604 | 0.307 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.608 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.492 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.375 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.489 |
LIG_TRFH_1 | 187 | 191 | PF08558 | 0.336 |
LIG_UBA3_1 | 362 | 370 | PF00899 | 0.453 |
LIG_WRC_WIRS_1 | 403 | 408 | PF05994 | 0.411 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.584 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.612 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.604 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.618 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.304 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.662 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.687 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.481 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.492 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.483 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.478 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.437 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.502 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.419 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.497 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.613 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.586 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.627 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.365 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.428 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.426 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.565 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.497 |
MOD_LATS_1 | 317 | 323 | PF00433 | 0.331 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.440 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.469 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.591 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.688 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.495 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.592 |
MOD_PK_1 | 356 | 362 | PF00069 | 0.455 |
MOD_PKA_1 | 319 | 325 | PF00069 | 0.451 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.697 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.419 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.593 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.525 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.695 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.431 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.310 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.439 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.428 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.435 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.473 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.517 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.592 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.595 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.377 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.353 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.473 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.310 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.290 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.566 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.536 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.559 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.645 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.470 |
MOD_SUMO_rev_2 | 135 | 143 | PF00179 | 0.687 |
MOD_SUMO_rev_2 | 38 | 46 | PF00179 | 0.709 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.616 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 361 | 366 | PF00026 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBI6 | Leptomonas seymouri | 47% | 98% |
A0A0S4JJJ8 | Bodo saltans | 30% | 100% |
A0A1X0P1I4 | Trypanosomatidae | 32% | 100% |
A0A1X0P1L0 | Trypanosomatidae | 32% | 100% |
A0A3R7NR23 | Trypanosoma rangeli | 32% | 100% |
A0A3S5H7N5 | Leishmania donovani | 73% | 99% |
A4I5T4 | Leishmania infantum | 73% | 99% |
C9ZR56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B129 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 99% |
Q4Q736 | Leishmania major | 73% | 100% |
V5DNZ0 | Trypanosoma cruzi | 31% | 100% |