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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q0Y0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.645 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 331 | 333 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.699 |
DEG_COP1_1 | 318 | 329 | PF00400 | 0.626 |
DOC_CYCLIN_RxL_1 | 520 | 527 | PF00134 | 0.603 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 17 | 26 | PF00134 | 0.696 |
DOC_PP1_RVXF_1 | 521 | 527 | PF00149 | 0.602 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.554 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.646 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 140 | 147 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 162 | 172 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 205 | 215 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 222 | 232 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 254 | 259 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 472 | 478 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 99 | 107 | PF00244 | 0.646 |
LIG_Actin_WH2_2 | 265 | 280 | PF00022 | 0.685 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.695 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.690 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.667 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.548 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.599 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.556 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.628 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.811 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.667 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.565 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.563 |
LIG_LIR_Apic_2 | 469 | 473 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.614 |
LIG_PDZ_Class_1 | 531 | 536 | PF00595 | 0.665 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.617 |
LIG_SH2_NCK_1 | 182 | 186 | PF00017 | 0.698 |
LIG_SH2_PTP2 | 339 | 342 | PF00017 | 0.557 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.740 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.550 |
LIG_SH2_SRC | 339 | 342 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.675 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.759 |
LIG_SH3_2 | 160 | 165 | PF14604 | 0.662 |
LIG_SH3_2 | 172 | 177 | PF14604 | 0.644 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.664 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.657 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.680 |
LIG_TRAF2_1 | 342 | 345 | PF00917 | 0.613 |
LIG_TRAF2_1 | 357 | 360 | PF00917 | 0.447 |
LIG_TYR_ITIM | 56 | 61 | PF00017 | 0.613 |
LIG_WRC_WIRS_1 | 517 | 522 | PF05994 | 0.656 |
MOD_CDK_SPK_2 | 122 | 127 | PF00069 | 0.661 |
MOD_CDK_SPK_2 | 168 | 173 | PF00069 | 0.724 |
MOD_CDK_SPK_2 | 225 | 230 | PF00069 | 0.794 |
MOD_CDK_SPxK_1 | 435 | 441 | PF00069 | 0.695 |
MOD_CDK_SPxxK_3 | 263 | 270 | PF00069 | 0.624 |
MOD_CDK_SPxxK_3 | 435 | 442 | PF00069 | 0.756 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.748 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.837 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.769 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.555 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.611 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.782 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.581 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.669 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.803 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.739 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.696 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.645 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.598 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.809 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.727 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.544 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.645 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.580 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.755 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.529 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.662 |
MOD_Cter_Amidation | 477 | 480 | PF01082 | 0.711 |
MOD_Cter_Amidation | 500 | 503 | PF01082 | 0.728 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.752 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.642 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.735 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.672 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.815 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.651 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.784 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.595 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.626 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.677 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.755 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.624 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.769 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.670 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.739 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.730 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.671 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.726 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.780 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.664 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.670 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.487 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.784 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.732 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.538 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.776 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.653 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.643 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.629 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.714 |
MOD_LATS_1 | 23 | 29 | PF00433 | 0.643 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.776 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.703 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.657 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.735 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.635 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.696 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.492 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.617 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.788 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.733 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.646 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.672 |
MOD_PK_1 | 254 | 260 | PF00069 | 0.617 |
MOD_PKA_1 | 441 | 447 | PF00069 | 0.702 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.797 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.693 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.726 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.722 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.710 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.709 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.732 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.672 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.788 |
MOD_PKB_1 | 247 | 255 | PF00069 | 0.775 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.734 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.510 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.585 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.604 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.677 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.642 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.793 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.658 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.652 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.659 |
MOD_SUMO_rev_2 | 124 | 131 | PF00179 | 0.623 |
TRG_DiLeu_BaEn_4 | 344 | 350 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 76 | 82 | PF01217 | 0.718 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.684 |
TRG_NLS_Bipartite_1 | 487 | 503 | PF00514 | 0.614 |
TRG_NLS_MonoExtC_3 | 445 | 450 | PF00514 | 0.602 |
TRG_NLS_MonoExtC_3 | 498 | 503 | PF00514 | 0.613 |
TRG_NLS_MonoExtN_4 | 446 | 453 | PF00514 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.713 |
TRG_Pf-PMV_PEXEL_1 | 347 | 352 | PF00026 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 356 | 360 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0U4 | Leptomonas seymouri | 39% | 100% |
A0A3Q8IPF2 | Leishmania donovani | 84% | 97% |
A4HPV1 | Leishmania braziliensis | 54% | 98% |
A4IE40 | Leishmania infantum | 83% | 97% |
E9ATL8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |