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 | yes | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q1L6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.418 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.394 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.462 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.787 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.798 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.496 |
DEG_COP1_1 | 77 | 85 | PF00400 | 0.562 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.650 |
DEG_SPOP_SBC_1 | 15 | 19 | PF00917 | 0.679 |
DEG_SPOP_SBC_1 | 266 | 270 | PF00917 | 0.398 |
DEG_SPOP_SBC_1 | 277 | 281 | PF00917 | 0.259 |
DOC_CYCLIN_RxL_1 | 418 | 428 | PF00134 | 0.569 |
DOC_MAPK_gen_1 | 284 | 293 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 284 | 293 | PF00069 | 0.335 |
DOC_PP2B_PxIxI_1 | 69 | 75 | PF00149 | 0.454 |
DOC_PP4_FxxP_1 | 220 | 223 | PF00568 | 0.423 |
DOC_PP4_FxxP_1 | 58 | 61 | PF00568 | 0.542 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.588 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.780 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.775 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.477 |
LIG_eIF4E_1 | 52 | 58 | PF01652 | 0.478 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.404 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.477 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.409 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.475 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.371 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.453 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.719 |
LIG_LIR_Apic_2 | 218 | 223 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 324 | 335 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 391 | 400 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 324 | 330 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.523 |
LIG_MYND_1 | 215 | 219 | PF01753 | 0.449 |
LIG_NRBOX | 244 | 250 | PF00104 | 0.437 |
LIG_Pex14_1 | 54 | 58 | PF04695 | 0.478 |
LIG_REV1ctd_RIR_1 | 207 | 214 | PF16727 | 0.317 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.512 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.398 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.344 |
LIG_SH2_NCK_1 | 234 | 238 | PF00017 | 0.281 |
LIG_SH2_PTP2 | 339 | 342 | PF00017 | 0.385 |
LIG_SH2_SRC | 368 | 371 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.385 |
LIG_SH3_2 | 43 | 48 | PF14604 | 0.560 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.698 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.654 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.370 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.489 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.746 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.538 |
LIG_SUMO_SIM_anti_2 | 252 | 258 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 252 | 258 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 9 | 19 | PF11976 | 0.496 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.449 |
LIG_WRC_WIRS_1 | 309 | 314 | PF05994 | 0.449 |
LIG_WRC_WIRS_1 | 7 | 12 | PF05994 | 0.492 |
MOD_CDK_SPxxK_3 | 480 | 487 | PF00069 | 0.784 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.657 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.691 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.430 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.466 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.575 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.716 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.563 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.449 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.447 |
MOD_CMANNOS | 121 | 124 | PF00535 | 0.415 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.739 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.704 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.616 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.281 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.437 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.437 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.462 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.776 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.774 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.721 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.439 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.439 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.400 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.385 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.658 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.469 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.786 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.584 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.346 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.572 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.599 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.327 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.383 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.454 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.434 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.441 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.673 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.541 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.464 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.482 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.242 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.398 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.503 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.600 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.441 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.767 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.563 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.780 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.442 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.421 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.404 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.545 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.573 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.595 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.544 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.420 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.666 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.654 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.411 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.341 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.478 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.469 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.754 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.782 |
TRG_AP2beta_CARGO_1 | 303 | 313 | PF09066 | 0.451 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_1 | 304 | 309 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_2 | 390 | 396 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_4 | 252 | 258 | PF01217 | 0.398 |
TRG_DiLeu_LyEn_5 | 212 | 217 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.330 |
TRG_NLS_MonoExtN_4 | 484 | 491 | PF00514 | 0.764 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 93 | 98 | PF00026 | 0.547 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILN3 | Leptomonas seymouri | 55% | 100% |
A0A0S4J806 | Bodo saltans | 36% | 100% |
A0A1X0P7Q2 | Trypanosomatidae | 43% | 100% |
A0A3Q8IG26 | Leishmania donovani | 90% | 100% |
A0A422N1S4 | Trypanosoma rangeli | 40% | 100% |
A4HP74 | Leishmania braziliensis | 72% | 100% |
A4IDH9 | Leishmania infantum | 90% | 100% |
D0A370 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ASY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BGE6 | Trypanosoma cruzi | 43% | 100% |