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: E9B480
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 | 264 | 268 | PF00656 | 0.452 |
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.528 |
CLV_MEL_PAP_1 | 628 | 634 | PF00089 | 0.617 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 468 | 470 | PF00082 | 0.235 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 557 | 559 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 464 | 470 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.364 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.288 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.354 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.296 |
DEG_SPOP_SBC_1 | 526 | 530 | PF00917 | 0.530 |
DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.269 |
DOC_MAPK_gen_1 | 468 | 475 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 654 | 663 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.435 |
DOC_MAPK_RevD_3 | 551 | 564 | PF00069 | 0.317 |
DOC_PP4_FxxP_1 | 513 | 516 | PF00568 | 0.448 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.416 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 174 | 184 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 287 | 297 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 435 | 444 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 597 | 601 | PF00244 | 0.532 |
LIG_deltaCOP1_diTrp_1 | 275 | 285 | PF00928 | 0.425 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.595 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.468 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.407 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.475 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.436 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.605 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.391 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.520 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.545 |
LIG_LIR_Apic_2 | 511 | 516 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 300 | 310 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 322 | 332 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 491 | 500 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 546 | 556 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 470 | 474 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 622 | 628 | PF02991 | 0.491 |
LIG_NRBOX | 458 | 464 | PF00104 | 0.448 |
LIG_PCNA_PIPBox_1 | 614 | 623 | PF02747 | 0.567 |
LIG_PCNA_yPIPBox_3 | 614 | 623 | PF02747 | 0.508 |
LIG_SH2_CRK | 539 | 543 | PF00017 | 0.271 |
LIG_SH2_PTP2 | 137 | 140 | PF00017 | 0.530 |
LIG_SH2_PTP2 | 625 | 628 | PF00017 | 0.573 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 545 | 549 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 621 | 625 | PF00017 | 0.529 |
LIG_SH2_STAT3 | 500 | 503 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.573 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.458 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.460 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.530 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.604 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.664 |
LIG_Sin3_3 | 166 | 173 | PF02671 | 0.260 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 165 | 171 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 522 | 533 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 540 | 548 | PF11976 | 0.382 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.271 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.433 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.510 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.686 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.522 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.269 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.611 |
MOD_Cter_Amidation | 466 | 469 | PF01082 | 0.269 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.520 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.596 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.413 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.514 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.404 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.287 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.545 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.533 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.650 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.463 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.426 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.489 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.575 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.364 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.526 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.385 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.658 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.362 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.517 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.603 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.447 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.273 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.443 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.598 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.409 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.371 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.402 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.653 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.479 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.669 |
MOD_PIKK_1 | 610 | 616 | PF00454 | 0.553 |
MOD_PKA_1 | 182 | 188 | PF00069 | 0.255 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.400 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.276 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.413 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.496 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.287 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.552 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.526 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.453 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.447 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.351 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.533 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.400 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.269 |
MOD_Plk_2-3 | 261 | 267 | PF00069 | 0.450 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.298 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.264 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.441 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.461 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.269 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.490 |
MOD_SUMO_for_1 | 45 | 48 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 34 | 41 | PF00179 | 0.600 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.273 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.310 |
TRG_DiLeu_BaLyEn_6 | 284 | 289 | PF01217 | 0.259 |
TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.330 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 422 | 425 | PF00400 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.290 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8D8 | Leptomonas seymouri | 57% | 86% |
A0A1X0P3T2 | Trypanosomatidae | 40% | 100% |
A0A3S5ISG6 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X6Z1 | Leishmania donovani | 89% | 100% |
A4HLV3 | Leishmania braziliensis | 72% | 100% |
D0A670 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AHQ9 | Leishmania infantum | 88% | 87% |
Q4Q3U6 | Leishmania major | 88% | 100% |
V5BP75 | Trypanosoma cruzi | 40% | 100% |