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: A0A3S7WZZ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.639 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.584 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.602 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.597 |
DOC_CKS1_1 | 269 | 274 | PF01111 | 0.725 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.600 |
DOC_CYCLIN_RxL_1 | 31 | 42 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 290 | 300 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 462 | 471 | PF00069 | 0.729 |
DOC_MAPK_MEF2A_6 | 293 | 300 | PF00069 | 0.502 |
DOC_MAPK_NFAT4_5 | 293 | 301 | PF00069 | 0.509 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.754 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.403 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 264 | 270 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.625 |
LIG_Actin_WH2_2 | 147 | 162 | PF00022 | 0.680 |
LIG_APCC_ABBAyCdc20_2 | 44 | 50 | PF00400 | 0.413 |
LIG_BIR_III_2 | 152 | 156 | PF00653 | 0.630 |
LIG_BRCT_BRCA1_1 | 125 | 129 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 451 | 455 | PF00533 | 0.780 |
LIG_CSL_BTD_1 | 120 | 123 | PF09270 | 0.667 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.730 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.629 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.644 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.669 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.628 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.704 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.751 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.751 |
LIG_LIR_Apic_2 | 238 | 244 | PF02991 | 0.616 |
LIG_LIR_Apic_2 | 267 | 272 | PF02991 | 0.738 |
LIG_LIR_Gen_1 | 126 | 134 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 149 | 159 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.726 |
LIG_MLH1_MIPbox_1 | 125 | 129 | PF16413 | 0.561 |
LIG_MYND_1 | 22 | 26 | PF01753 | 0.394 |
LIG_NRBOX | 204 | 210 | PF00104 | 0.676 |
LIG_NRBOX | 295 | 301 | PF00104 | 0.611 |
LIG_Pex14_1 | 125 | 129 | PF04695 | 0.583 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.656 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.549 |
LIG_SH3_1 | 313 | 319 | PF00018 | 0.736 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.650 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.641 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.527 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.773 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.736 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.681 |
LIG_SUMO_SIM_par_1 | 168 | 176 | PF11976 | 0.704 |
LIG_SUMO_SIM_par_1 | 296 | 302 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 90 | 96 | PF11976 | 0.424 |
LIG_SxIP_EBH_1 | 69 | 82 | PF03271 | 0.406 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.657 |
LIG_TYR_ITIM | 299 | 304 | PF00017 | 0.506 |
LIG_WRC_WIRS_1 | 266 | 271 | PF05994 | 0.549 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.636 |
LIG_WW_3 | 310 | 314 | PF00397 | 0.681 |
MOD_CDK_SPK_2 | 135 | 140 | PF00069 | 0.556 |
MOD_CDK_SPK_2 | 220 | 225 | PF00069 | 0.498 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.390 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.755 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.563 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.707 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.810 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.768 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.382 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.726 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.638 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.618 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.676 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.760 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.599 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.641 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.504 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.625 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.632 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.560 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.587 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.792 |
MOD_GlcNHglycan | 408 | 412 | PF01048 | 0.785 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.400 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.526 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.689 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.623 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.621 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.678 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.600 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.599 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.499 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.648 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.630 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.541 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.646 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.776 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.836 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.394 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.645 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.558 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.628 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.654 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.550 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.553 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.543 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.573 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.536 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.418 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.432 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.533 |
MOD_PK_1 | 225 | 231 | PF00069 | 0.708 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.606 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.683 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.665 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.647 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.566 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.562 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.389 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.580 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.517 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.606 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.524 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.602 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.726 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.402 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.746 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.724 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.392 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.587 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.652 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.808 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.783 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.710 |
TRG_DiLeu_BaEn_4 | 466 | 472 | PF01217 | 0.590 |
TRG_DiLeu_BaLyEn_6 | 154 | 159 | PF01217 | 0.634 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.721 |
TRG_Pf-PMV_PEXEL_1 | 329 | 334 | PF00026 | 0.633 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H2 | Leptomonas seymouri | 30% | 100% |
A4HEY8 | Leishmania braziliensis | 64% | 100% |
A4I262 | Leishmania infantum | 99% | 100% |
E9AYB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q961 | Leishmania major | 88% | 100% |