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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X6Z1
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 11 |
GO:0006448 | regulation of translational elongation | 7 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009889 | regulation of biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010468 | regulation of gene expression | 5 | 11 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 11 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 11 |
GO:0017182 | peptidyl-diphthamide metabolic process | 7 | 11 |
GO:0017183 | peptidyl-diphthamide biosynthetic process from peptidyl-histidine | 4 | 11 |
GO:0018193 | peptidyl-amino acid modification | 5 | 11 |
GO:0018202 | peptidyl-histidine modification | 6 | 11 |
GO:0019222 | regulation of metabolic process | 3 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0031323 | regulation of cellular metabolic process | 4 | 11 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 11 |
GO:0034248 | regulation of amide metabolic process | 5 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 |
GO:0051246 | regulation of protein metabolic process | 5 | 11 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0080090 | regulation of primary metabolic process | 4 | 11 |
GO:1900247 | regulation of cytoplasmic translational elongation | 8 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 11 |
GO:0090560 | 2-(3-amino-3-carboxypropyl)histidine synthase activity | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.354 |
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.516 |
CLV_MEL_PAP_1 | 628 | 634 | PF00089 | 0.663 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 468 | 470 | PF00082 | 0.261 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 557 | 559 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 464 | 470 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.602 |
CLV_Separin_Metazoa | 172 | 176 | PF03568 | 0.348 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.323 |
DEG_SPOP_SBC_1 | 269 | 273 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.394 |
DOC_MAPK_gen_1 | 468 | 475 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.460 |
DOC_MAPK_RevD_3 | 551 | 564 | PF00069 | 0.355 |
DOC_PP2B_PxIxI_1 | 207 | 213 | PF00149 | 0.375 |
DOC_PP4_FxxP_1 | 513 | 516 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.633 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 227 | 237 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 288 | 297 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 435 | 444 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 588 | 596 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 78 | 83 | PF00244 | 0.657 |
LIG_deltaCOP1_diTrp_1 | 277 | 286 | PF00928 | 0.447 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.588 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.473 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.502 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.475 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.323 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.575 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.542 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.622 |
LIG_GBD_Chelix_1 | 177 | 185 | PF00786 | 0.382 |
LIG_LIR_Apic_2 | 511 | 516 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 300 | 310 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 322 | 332 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 491 | 499 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 546 | 556 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 240 | 244 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 37 | 41 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 470 | 474 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 622 | 628 | PF02991 | 0.544 |
LIG_NRBOX | 458 | 464 | PF00104 | 0.475 |
LIG_SH2_PTP2 | 138 | 141 | PF00017 | 0.550 |
LIG_SH2_PTP2 | 625 | 628 | PF00017 | 0.632 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 545 | 549 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.632 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.572 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.485 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.550 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.701 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.683 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 522 | 529 | PF11976 | 0.492 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.311 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.608 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.459 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.372 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.722 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.609 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.305 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.619 |
MOD_Cter_Amidation | 466 | 469 | PF01082 | 0.305 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.530 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.519 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.541 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.655 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.643 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.648 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.402 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.506 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.414 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.324 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.324 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.593 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.586 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.747 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.582 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.391 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.505 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.601 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.567 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.396 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.549 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.641 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.639 |
MOD_LATS_1 | 76 | 82 | PF00433 | 0.602 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.479 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.309 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.367 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.641 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.404 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.429 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.547 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.702 |
MOD_PIKK_1 | 610 | 616 | PF00454 | 0.604 |
MOD_PK_1 | 247 | 253 | PF00069 | 0.622 |
MOD_PKA_1 | 227 | 233 | PF00069 | 0.433 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.314 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.509 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.521 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.324 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.372 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.576 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.662 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.568 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.517 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.312 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.411 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.305 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.530 |
MOD_SUMO_rev_2 | 34 | 41 | PF00179 | 0.598 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.632 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 422 | 425 | PF00400 | 0.331 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8D8 | Leptomonas seymouri | 55% | 86% |
A0A1X0P3T2 | Trypanosomatidae | 39% | 100% |
A0A3S5ISG6 | Trypanosoma rangeli | 41% | 100% |
A4HLV3 | Leishmania braziliensis | 73% | 100% |
D0A670 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AHQ9 | Leishmania infantum | 98% | 100% |
E9B480 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q3U6 | Leishmania major | 92% | 100% |
V5BP75 | Trypanosoma cruzi | 40% | 100% |